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Merlintrader Biotech Calendar

Biotech Catalyst Calendar 2026: PDUFA & FDA Dates

FDA decisions, PDUFA dates, advisory committees and clinical-trial readouts for publicly traded biotech stocks.

Tables updated: October 22, 2026; glossary reviewed: September 19, 2026

This is Merlintrader’s dedicated biotech catalyst calendar. It tracks upcoming FDA decisions, PDUFA target dates, advisory committee meetings, NDA and BLA milestones, regulatory submissions and major clinical-trial readouts for publicly traded biotech and healthcare companies, including selected non-U.S. listings with FDA milestones.

Each entry is designed to show the expected timing, event type, company context and available source trail. The tables separate confirmed dates, conference ranges, estimated company windows and recent history. Each entry links to its sources; the embedded calendar provides a wider archive.

Catalyst dates can change, FDA decisions can arrive early or late and clinical readouts can be postponed. Always confirm each event against company filings, official press releases and regulatory sources before making any trading or investment decision.

Calendar: upcoming catalysts and history

These tables are an editorial selection of events supported by primary sources. Regulatory dates, confirmed presentations and company windows are separated; passed or completed events appear only in history, with their verified status stated. A PDUFA date is a review goal, not a promise of approval.

Data as of October 22, 2026, 18:49 Europe/Rome — 766 upcoming company events or open windows — 223 recent historical events. Confirmed dates and company estimates remain distinct.

Confirmed regulatory deadlines: 59 events

Date / windowTickerCompanyEventStatusSources
2026-10-30$INOInovio Pharmaceuticals, Inc.INO-3107, DNA immunotherapy — recurrent respiratory papillomatosis in adults.Confirmed datePrimary source
2026-11-01$AGIOAgios Pharmaceuticals, Inc.Pyrukynd (mitapivat) — sickle cell disease, accelerated approval pathway. Program detail: PYRUKYND (mitapivat); NDA.Confirmed datePrimary source
2026-11-10$NRXPNRx Pharmaceuticals, Inc.FDA goal date (GDUFA) for the Abbreviated New Drug Application (ANDA) of NRx's preservative-free intravenous ketamine. The FDA reclassified the pending amendment from major to minor and revised the goal date to November 10, 2026 (announced September 15, 2026). On October 15, 2026 the company reported a labeling discipline review letter requesting only minor changes. A goal date is not a decision.Confirmed dateSEC filing
Supporting source
2026-11-14$BTAIBioXcel Therapeutics, Inc.CHAPTER 11 / NASDAQ SUSPENSION — BioXcel filed Chapter 11 on August 27, 2026. Its September 1 filing announced Nasdaq trading suspension effective September 8, with no appeal planned. Igalmi at-home-use sNDA: November 14, 2026 PDUFA retained as a drug regulatory milestone. A favorable FDA decision does not establish recovery for common shareholders. Proposed asset sale is not treated here as a completed transaction.WARNING: CHAPTER 11 / NASDAQ SUSPENSIONConfirmed datePrimary source
Supporting source
Supporting source
2026-11-14$CYTKCYTOKINETICS INCMYQORZO (aficamten) — obstructive hypertrophic cardiomyopathy; extension based on the MAPLE-HCM trial.Confirmed datePrimary source
2026-11-14$SMMTSummit Therapeutics Inc.ivonescimab (SMT112) — EGFR-mutated non-squamous NSCLC, after TKI, in combination with chemotherapyConfirmed datePrimary source
2026-11-22$CAPRCAPRICOR THERAPEUTICS, INC.deramiocel (CAP-1002), cell therapy — Duchenne muscular dystrophy; refined proposed indication focused on upper limb function. FDA review of the BLA major amendment includes 24-month HOPE-3 open-label extension data and robustness analyses. On 24 August 2026 Capricor announced a three-month extension from 22 August to 22 November 2026. The target date is not an approval.Confirmed datePrimary source
2026-11-22$SVRASavara Inc.Molbreevi (molgramostim), inhalation solution — autoimmune pulmonary alveolar proteinosis. FDA review date extended by three months for a major amendment.Confirmed datePrimary source
2026-11-25$SNYSanofivenglustat, oral glucosylceramide synthase inhibitor — Gaucher disease type 3, neurological manifestations.Confirmed datePrimary source
2026-11-27$BBIOBridgeBio Pharma, Inc.BBP-418 — limb-girdle muscular dystrophy LGMD2I/R9.Confirmed datePrimary source
2026-11-27$GSKGSKneladalkib (NVL-655) — advanced ALK-positive NSCLC, previously treated with TKI. Formerly a Nuvalent asset, acquired by GSK on July 15, 2026.Confirmed datePrimary source
Supporting source
2026-11-27$RPRXRoyalty Pharma plcneladalkib — ALK-positive non-small cell lung cancer; royalty interest. FDA target action date: November 27, 2026.Confirmed datePrimary source
2026-11-28$PYPDPolyPid Ltd.D-PLEX100, local prolonged-release doxycycline depot — prevention of surgical site infections in colorectal surgeryConfirmed datePrimary source
2026-11-30$COGTCogent Biosciences, Inc.bezuclastinib, with sunitinib — gastrointestinal stromal tumours previously treated with imatinib. Merlintrader stock hub: COGT.Confirmed datePrimary source
COGT stock hub
2026-11-30$RHHBYF. Hoffmann-La Roche Ltdgiredestrant — adjuvant treatment of ER-positive, HER2-negative early breast cancer, lidERA trial.Confirmed datePrimary source
2026-11-30$VRTXVERTEX PHARMACEUTICALS INCORPORATEDpovetacicept, dual BAFF and APRIL inhibitor — IgA nephropathy, accelerated approval pathway.Confirmed datePrimary source
2026-11-30$ZLABZai Lab Limitedpovetacicept — IgA nephropathy; Vertex partner. FDA target action date: November 30, 2026.Confirmed datePrimary source
ZLAB stock hub
2026-12-12$ANABANAPTYSBIO, INCimsidolimab — generalized pustular psoriasis; Vanda partner. FDA target action date: December 12, 2026.Confirmed datePrimary source
ANAB stock hub
2026-12-12$VNDAVanda Pharmaceuticals Inc.imsidolimab, IL-36R antagonist — generalized pustular psoriasis. Molecule originated by AnaptysBio; BLA held by Vanda.Confirmed datePrimary source
2026-12-17$CORTCorcept Therapeutics Incorporatedrelacorilant, selective glucocorticoid receptor antagonist — Cushing's syndrome. NDA resubmitted on June 17, 2026 after a CRL on this indication.Confirmed datePrimary source
2026-12-18$CAMXCamurus ABCAM2029 (Oclaiz), acromegaly NDA resubmission: FDA target action date confirmed for December 18, 2026. A review target is not an approval. Nasdaq Stockholm ticker CAMX.Confirmed datePrimary source
2026-12-18$RHHBYF. Hoffmann-La Roche Ltdgiredestrant + everolimus — ER+/HER2− advanced or metastatic breast cancer with an ESR1 mutation, following progression on or after prior endocrine therapy.Confirmed datePrimary source
2026-12-22$MLYSMineralys Therapeutics, Inc.lorundrostat — hypertension in adults, in combination with other antihypertensives. Program detail: lorundrostat; NDA. Merlintrader stock hub: MLYS.Confirmed datePrimary source
MLYS stock hub
2026-12-23$GILDGILEAD SCIENCES, INC.anito-cel (anitocabtagene autoleucel), anti-BCMA CAR-T — relapsed or refractory multiple myeloma, fourth line. BLA filed by Arcellx, acquired by Gilead on April 28, 2026.Confirmed datePrimary source
2026-12-27$PRAXPraxis Precision Medicines, Inc.relutrigine — SCN2A and SCN8A developmental and epileptic encephalopathies (NDA). Date extended from September 27, 2026 for a major amendment.Confirmed datePrimary source
2026-12-27$VTRSViatris Inc.fast-acting meloxicam — moderate to severe acute pain, non-opioid analgesic. Merlintrader stock hub: VTRS.Confirmed datePrimary source
VTRS stock hub
2026-12-30$COGTCogent Biosciences, Inc.bezuclastinib monotherapy — non-advanced systemic mastocytosis. Merlintrader stock hub: COGT.Confirmed datePrimary source
COGT stock hub
4 January 2027$NUVBNUVATION BIO INCPDUFA: IBTROZI (taletrectinib) · advanced ROS1-positive non-small cell lung cancer (NSCLC). Company timing: January 4, 2027. FDA target action date; approval is not assured.Confirmed datePrimary source
2027-01-21$DYNDyne Therapeutics, Inc.z-rostudirsen (DYNE-251) — Duchenne muscular dystrophy amenable to exon 51 skipping. FDA target action date: January 21, 2027.Confirmed datePrimary source
2027-01-29$PRAXPraxis Precision Medicines, Inc.ulixacaltamide — essential tremor. FDA target action date: January 29, 2027.Confirmed datePrimary source
2027-02-04$BBIOBridgeBio Pharma, Inc.FDA accepted the NDA with Priority Review and assigned a February 4, 2027 PDUFA target, per the October 6 company announcement. Review acceptance is not approval.Confirmed datePrimary source
2027-02-12$BLTEBELITE BIO, INCtinlarebant — Stargardt disease type 1. FDA target action date: February 12, 2027.Confirmed datePrimary source
2027-02-23$ARQTArcutis Biotherapeutics, Inc.Zoryve cream 0.05% — atopic dermatitis, infants aged 3 to 24 months. FDA target action date: February 23, 2027.Confirmed datePrimary source
2027-02-27$CGEMCullinan Therapeutics, Inc.zipalertinib — EGFR exon 20 insertion non-small cell lung cancer. FDA target action date: February 27, 2027.Confirmed datePrimary source
2027-02-28$APMDApnimed, Inc.AD109 — obstructive sleep apnea. FDA target action date: February 28, 2027.Confirmed datePrimary source
2027-02-28$BMRNBioMarin Pharmaceutical Inc.Voxzogo (vosoritide) — full approval in children with achondroplasia. FDA target action date: February 28, 2027.Confirmed datePrimary source
2027-02-28$SRPTSarepta Therapeutics, Inc.AMONDYS 45 and VYONDYS 53 — Duchenne muscular dystrophy; traditional approval conversion. FDA target action date: February 28, 2027.Confirmed datePrimary source
2027-03-03$EXELEXELIXIS, INC.zanzalintinib + atezolizumab — previously treated metastatic colorectal cancer, STELLAR-303. New target March 3, 2027; December 3, 2026 is no longer an active deadline. FDA notified the company on September 10 that new safety and efficacy data constituted a major amendment; filing dated September 11.Confirmed datePrimary source
2027-03-10$NTLAIntellia Therapeutics, Inc.Lonvoguran ziclumeran (lonvo-z/NTLA-2002) for hereditary angioedema: BLA accepted with Priority Review, FDA PDUFA target March 10, 2027. Approval is not assured. One application, one event.Confirmed datePrimary source
Supporting source
2027-03-11$BMYBRISTOL MYERS SQUIBBReblozyl (luspatercept) — myelofibrosis-associated anemia. FDA target action date: March 11, 2027.Confirmed datePrimary source
2027-03-16$AQSTAquestive Therapeutics, Inc.FDA goal date (PDUFA) for the resubmitted NDA of Anaphylm (dibutepinephrine) sublingual film for the treatment of Type I allergic reactions, including anaphylaxis. The FDA accepted the resubmission, filed on September 16, 2026, as complete and classified it as a Class 2 response (announced October 15, 2026).Confirmed dateSEC filing
2027-03-22$MRKMerck & Co., Inc.Enflonsia (clesrovimab-cfor) — children entering a second RSV season at increased risk. FDA target action date: March 22, 2027.Confirmed datePrimary source
2027-03-25$UNCYUnicycive Therapeutics, Inc.PDUFA target action date for the resubmitted NDA of oxylanthanum carbonate (OLC), oral phosphate binder for hyperphosphatemia in patients with chronic kidney disease on dialysis. The FDA accepted the resubmission, filed after a Complete Response Letter in June 2026, as a Class II resubmission with a six-month review period from the resubmission date. The resubmission includes CMC data from a new third-party drug product manufacturing vendor; the company does not know whether the FDA will conduct a pre-approval inspection of that vendor.Confirmed dateFinviz (news)
2027-03-29$AQSTAquestive Therapeutics, Inc.FDA goal date (PDUFA) for the LIBERVANT (diazepam) buccal film application for patients aged 6 to 11 with seizure clusters, as cited in the October 14, 2026 Eton/Aquestive license announcement. Eton holds the exclusive U.S. commercial rights; Aquestive is the exclusive manufacturer and receives milestones and royalties.Confirmed datePrimary source
2027-03-29$ETONETON PHARMACEUTICALS INCFDA goal date (PDUFA) for the LIBERVANT (diazepam) buccal film application for patients aged 6 to 11 with seizure clusters. Eton licensed exclusive U.S. rights from Aquestive on October 13, 2026 ($10.0 million upfront, up to $47.5 million in milestones, mid-teens royalties).Confirmed datePrimary source
SEC filing
2027-03-31$ATRAAtara Biotherapeutics, Inc.FDA accepted the Class 2 resubmission of the tabelecleucel (tab-cel) Biologics License Application for Epstein-Barr virus-positive post-transplant lymphoproliferative disease (EBV+ PTLD), announced October 14, 2026 by partner Pierre Fabre Pharmaceuticals. New PDUFA goal date: March 31, 2027.Confirmed datePrimary source
2027-04-01$HRMYHarmony Biosciences Holdings, Inc.pitolisant GR — narcolepsy. FDA target action date: April 1, 2027.Confirmed datePrimary source
14 April 2027$INBXINHIBRX BIOSCIENCES INCPDUFA: ozekibart (INBRX-109) · Conventional chondrosarcoma. Company timing: April 14, 2027. FDA target action date; approval is not assured.Confirmed datePrimary source
2027-04-23$PHVSPharvaris N.V.deucrictibant IR — on-demand treatment of hereditary angioedema attacks. FDA target action date: April 23, 2027.Confirmed datePrimary source
2027-04-23$RPRXRoyalty Pharma plcdeucrictibant IR — hereditary angioedema; royalty interest. FDA target action date: April 23, 2027.Confirmed datePrimary source
2027-04-24$ORGOOrganogenesis Holdings Inc.ReNu — symptomatic knee osteoarthritis. FDA target action date: April 24, 2027.Confirmed datePrimary source
2027-04-28$IMNMIMMUNOME, INC.varegacestat — desmoid tumors in adults. FDA target action date: April 28, 2027.Confirmed datePrimary source
2027-05-01$AXSMAxsome Therapeutics, Inc.AXS-12 (reboxetine) — narcolepsy. FDA target action date: May 1, 2027.Confirmed datePrimary source
2027-05-08$BBIOBridgeBio Pharma, Inc.encaleret — autosomal dominant hypocalcemia type 1. FDA target action date: May 8, 2027.Confirmed datePrimary source
2027-05-13$BMYBRISTOL MYERS SQUIBBmezigdomide with carfilzomib and dexamethasone — relapsed/refractory multiple myeloma. FDA target action date: May 13, 2027.Confirmed datePrimary source
2027-05-27$ZBIOZenas BioPharma, Inc.obexelimab — IgG4-related disease. FDA target action date: May 27, 2027.Confirmed datePrimary source
2027-06-14$URGNUROGEN PHARMA LTDPDUFA: UGN-103 (mitomycin) for intravesical solution · recurrent low-grade intermediate-risk non-muscle invasive bladder cancer (LG-IR-NMIBC). UroGen announced on October 19, 2026 that the FDA accepted the NDA, with a PDUFA target action date of June 14, 2027. Supported by the Phase 3 UTOPIA trial.Confirmed datePrimary source
2027-06-24$UTHRUNITED THERAPEUTICS CORPORATIONralinepag — pulmonary arterial hypertension. FDA target action date: June 24, 2027.Confirmed datePrimary source
2027-06-29$COGTCogent BiosciencesBezuclastinib NDA in advanced systemic mastocytosis (AdvSM): FDA target action date June 29, 2027, announced September 15. Separate from GIST November 30 and nonadvanced SM December 30, 2026. Approval is not assured.Confirmed datePrimary source
COGT stock hub
Full calendar

Want to see the rest of the catalysts?

Below: the remaining confirmed regulatory deadlines, clinical and corporate events with a confirmed day, conferences, company windows and recent history, every entry with its primary source, plus the full event calendar, the Catalyst Lookup and the glossary.

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Clinical and corporate events with a confirmed day: 143 events

Date / windowTickerCompanyEventStatusSources
October 22, 2026$ABCLAbCellera Biologics Inc.ABCL635 TMS poster P-92, October 22 at 6:15-7:15 p.m. PDT: new multiple-ascending-dose Phase 1 safety and Phase 2 patient-reported outcomes in menopausal vasomotor symptoms. This is a presentation of additional data, not the already announced initial Phase 2 topline.Confirmed datePrimary source
October 22, 2026$HUMAHumacyte, Inc.ASN Kidney Week late-breaking oral TH-OR113 presents V012 Phase 3 interim findings in women needing hemodialysis access on October 22, 4:40–4:50 p.m. Mountain Time. ATEV is compared with autogenous arteriovenous fistula.Confirmed dateCompany release
2026-10-22$ICUSeaStar MedicalASN late-breaking poster TH-PO1291: postapproval SAVE pediatric sepsis-associated AKI registry compared with a historical cohort, 10 a.m.–noon Mountain Time. Distinct from the adult pivotal trial.Confirmed datePrimary source
2026-10-22$IMUXImmunic, Inc.MSToronto2026 (10th Joint ACTRIMS-ECTRIMS Meeting), Poster Session 2, Thursday, October 22, 2026, 4:30–6:30 p.m. ET: paper poster P1273 with preclinical data on Nurr1-dependent neuronal survival and neuroprotective effects of vidofludimus calcium in murine MS models. Preclinical data, not a clinical readout.Confirmed datePrimary source
2026-10-22$KPTIKaryopharm Therapeutics Inc.End of the lender forbearance period at 11:59 p.m. Eastern on October 22, 2026, after the parties moved it on October 13 from October 15 (8-K filed October 14). The forbearance follows the missed principal installment of approximately $15.8 million due September 10 under the term loan; the defaults are not waived and the period can end earlier if specified termination events occur.Confirmed dateSEC filing
SEC filing
2026-10-22$LBRXLB Pharmaceuticals Inc.Craig-Hallum Biotech Catalyst Conference: virtual fireside chat at 10:00 a.m. ET and virtual one-on-one investor meetings on Thursday, October 22, 2026. Webcast on the company investor website. An investor conference appearance, not a data release.Confirmed datePrimary source
October 22, 2026$MAZEMaze Therapeutics, Inc.ASN poster TH-PO0213 on preclinical SLC6A19 inhibition and a protective proximal-tubule metabolic state relevant to MZE782, October 22, 10:00 am-noon MT. Not clinical efficacy data.Confirmed datePrimary source
2026-10-22$PYPDPolyPid Ltd.IDWeek 2026 (Washington, D.C.), Late Breaking Abstracts: Antimicrobials, oral presentation on Thursday, October 22, 2026 (session 10:30–11:45 a.m. ET): exploratory pooled microbiology analysis of SHIELD I, SHIELD II and the Phase 2 trial of D-PLEX100 (2,185 patients). Exploratory analysis of completed trials, not a new primary-endpoint result.Confirmed dateFinviz (news)
2026-10-22$VERAVera Therapeutics, Inc.Investor webcast on Thursday, October 22, 2026, at 4:30 p.m. ET to discuss the ORIGIN 3 final efficacy analysis of TRUTAKNA (atacicept-vymj) in IgA nephropathy, presented as a late-breaking oral in the ASN Kidney Week 2026 opening plenary. With Jonathan Barratt, PhD, FRCP (University of Leicester); live Q&A follows.Confirmed datePrimary source
2026-10-22$ZBIOZenas BioPharma, Inc.MSToronto MoonStone Phase 2 posters P1417, P1411 and P1455, 4:30–6:30 p.m. ET: 24-week relapsing-MS clinical results, serum biomarkers and PK/PD analyses, grouped as one same-program session.Confirmed datePrimary source
Supporting source
October 22, 2026$ZBIOZENAS BIOPHARMA INCMSToronto poster P1446, October 22, 4:30–6:30 p.m. ET: 24-week efficacy and safety of orelabrutinib 80 mg in the randomized Phase 2 RRMS study. Not a Phase 3 readout.Confirmed datePrimary source
Supporting source
2026-10-23$ALNYAlnylam Pharmaceuticals, Inc.ALN-HTT02 Phase 1 initial results at EHDN; presentation date October 23, 2026 announced in Q2 results.Confirmed datePrimary source
2026-10-23$ARDXArdelyx, Inc.ASN posters on hyperphosphatemia management: real-world tenapanor/phosphate-binder use, patient perspectives and cumulative morbidity/mortality; not a pivotal interventional readout.Confirmed dateCompany release
2026-10-23$CELCCelcuity Inc.ESMO poster 2237P: Phase 1b subgroup analyses in metastatic castration-resistant prostate cancer. Separate from the Phase 2 Q4 2026 readout.Confirmed datePrimary source
2026-10-23$EIKNEikon Therapeutics, Inc.ESMO Congress 2026 (Madrid) posters on Friday, October 23, 2026, 15:15 – 16:00: 1048P, Phase 1/2 study of the PARP1-selective inhibitor EIK1003 as monotherapy and with paclitaxel in advanced solid tumors; 1049P, Phase 1/2 study of EIK1003 with abiraterone in metastatic prostate cancer; 1060P, first-in-human Phase 1/2 study of the CNS-penetrant PARP1-selective inhibitor EIK1004 in advanced solid tumors with HRR mutations; 1010P, safety, tolerability and PK of the WRN inhibitor EIK1005. Full-text abstracts published October 18.Confirmed datePrimary source
2026-10-23$GSKGSK plcESMO Congress 2026 (Madrid, October 23-27), Friday, October 23, 15:15-16:00 CET, Poster Session: 1071P (S. Goel), EMBOLD PanTumor-101 safety and efficacy of risvutatug rezetecan (Ris-Rez), GSK's investigational B7-H3-targeted antibody-drug conjugate, as monotherapy during dose escalation in a global population with advanced/metastatic solid tumours; 1068P (J. Zugazagoitia), pooled analysis of interstitial lung disease cases among patients with advanced solid tumours who received Ris-Rez monotherapy.Confirmed datePrimary source
2026-10-23$INCYINCYTEESMO Congress 2026 (Madrid) rapid oral 1241RO, Friday, October 23, 10:15-11:45 a.m. ET (4:15-5:45 p.m. CET): preliminary efficacy of INCB123667 (CDK2 inhibition) with bevacizumab in recurrent epithelial ovarian cancer.Confirmed datePrimary source
2026-10-23$IOVAIovance Biotherapeutics, Inc.ESMO Congress 2026: proffered-paper oral presentation (abstract 2072O) of final results from the IOV-COM-202 study of lifileucel plus pembrolizumab in immune checkpoint inhibitor-naive advanced melanoma, Friday, October 23, 2026, 16:15–17:45 CEST; same day, poster 4359P on enrichment of putative tumor-reactive clones in NSCLC patients responding to lifileucel (single-cell analysis), 15:15–16:00 CEST.Confirmed datePrimary source
2026-10-23$KYTXKyverna Therapeutics, Inc.MSToronto oral presentation, 11:05–11:15 a.m. ET: updated safety and preliminary efficacy from an investigator-initiated Phase 1 study of miv-cel in progressive multiple sclerosis.Confirmed datePrimary source
Supporting source
October 23, 2026$MAZEMaze Therapeutics, Inc.ASN poster FR-PO0215 on preclinical SLC6A19 inhibition and reduced nephrotoxin uptake relevant to MZE782, October 23, 10:00 am-noon MT. Separate poster; not clinical efficacy data.Confirmed datePrimary source
2026-10-23$PROKProKidney Corp.ASN poster FR-PO0498: pooled Phase 2 safety/efficacy in CKD with diabetes among participants meeting key Phase 3 eligibility criteria, 10 a.m.–noon MDT; not Phase 3 efficacy results.Confirmed datePrimary source
2026-10-23$SCYXSCYNEXIS, Inc.SCY-247, the company's second-generation triterpenoid antifungal candidate, featured in an oral company pipeline presentation at IDWeek 2026 in Washington, D.C.: "SCY-247, a novel phase 2 IV/oral triterpenoid antifungal", session New Antimicrobials in the Pipeline, Friday, October 23, 2026 at 8:00 a.m. ET.Confirmed datePrimary source
October 23, 2026$TGTXTG THERAPEUTICS INCFirst Phase 1 azer-cel data in primary progressive multiple sclerosis: MSToronto late-breaking oral presentation O135, October 23, 10:45–10:55 a.m. ET. Abstract release October 21.Confirmed datePrimary source
2026-10-23$TNGXTango Therapeutics, Inc.PDAC-focused investor webcast and conference call on Friday, October 23, 2026, at 7:30 am ET to discuss the vopimetostat plus RAS(ON) inhibitor combination data that the company will present at ESMO 2026 (poster 3149P, October 25). Live webcast under Events & Presentations on the company website, replay for at least 30 days.Confirmed datePrimary source
23 October 2026$ZLABZAI LAB LTDZai Lab investor webcast on zocilurtatug pelitecan (zoci) at ESMO: October 23, 2026 at 08:00 ET / 20:00 HKT. Separate from the October 26 poster presentation; no results are inferred in advance. Calendar uses an all-day reminder with the announced start time in this description because no end time is published.Confirmed datePrimary source
ZLAB stock hub
2026-10-23$ZNTLZentalis Pharmaceuticals, Inc.ESMO Congress 2026 (Madrid) rapid oral presentation 1242RO (Rapid Oral Presentation — Gynecological Cancers: Ovarian), Friday, October 23, 2026, 4:15 p.m. – 5:45 p.m. CEST: overall survival from an interim analysis of DENALI Part 1b (GOG-3066) with azenosertib in platinum-resistant ovarian cancer. The published abstract reports, as of the September 2, 2025 data cutoff, median OS of 15.8 months (95% CI, 8.7–17.8) in the Cyclin E1-positive subgroup (n=48) and 7.5 months (95% CI, 5.8–12.3) in the Cyclin E1-negative subgroup (n=46), with no new safety signals; OS is a secondary endpoint and Cyclin E1 status was determined retrospectively. Distinct from the DENALI Part 2 readout.Confirmed datePrimary source
2026-10-24$AMGNAMGEN INCWebcast call for the investment community in conjunction with ESMO 2026 on Saturday, October 24, 2026, at 11:30 a.m. PT, on Amgen's oncology portfolio and selected data presented at the congress. An investor event, not a new data release.Confirmed datePrimary source
2026-10-24$CELCCelcuity Inc.ESMO oral presentation of VIKTORIA-1 subgroup analyses in advanced breast cancer. Abstract release scheduled October 19.Confirmed datePrimary source
2026-10-24$CLYMClimb Bio IncASN oral presentation of preliminary PrisMN Phase 2 safety and efficacy data in primary membranous nephropathy, 5:30–5:40 p.m. Mountain Time.Confirmed datePrimary source
2026-10-24$CMPXCompass Therapeutics, Inc.COMPANION-002 tovecimig oral presentation at ESMO 2026. Confirmed date: session on October 24, 2026, 10:15–11:45 a.m. CET; individual presentation time not stated. Compass Therapeutics will present results of the randomized Phase 2/3 COMPANION-002 trial of tovecimig plus paclitaxel in advanced biliary tract cancer at ESMO on October 24, 2026.Confirmed datePrimary source
2026-10-24$GSKGSK plcESMO Congress 2026 (Madrid), Saturday, October 24, 8:30-10:00 CET, Rapid Oral Session: late-breaking LBA41 (V. Salutari), updated results with longer follow-up from the global Phase I BEHOLD-1 study of mocertatug rezetecan (Mo-Rez), GSK's investigational B7-H4-targeted antibody-drug conjugate, in platinum-resistant ovarian cancer; 1248RO (S. Lheureux), BEHOLD-1 exploratory analysis of biomarkers associated with Mo-Rez response in platinum-resistant ovarian cancer.Confirmed datePrimary source
2026-10-24$INCYINCYTEESMO Congress 2026 (Madrid) rapid oral 1954RO, Saturday, October 24, 2:30-4:00 a.m. ET (8:30-10:00 a.m. CET): INCA33890, a TGFβR2xPD-1 bispecific antibody, with standard-of-care anticancer therapies in microsatellite stable colorectal cancer.Confirmed datePrimary source
2026-10-24$IOVAIovance Biotherapeutics, Inc.ESMO Congress 2026: two posters on Saturday, October 24, 2026, 12:00–12:45 CEST, in anti-PD-1-resistant advanced melanoma: 2117P, indirect comparison of overall survival between lifileucel and standard of care in US real-world settings; 2125P, matching-adjusted indirect comparison of lifileucel versus nivolumab plus relatlimab.Confirmed datePrimary source
2026-10-24$LLYEli Lilly and CompanyESMO Congress 2026 (Madrid, October 23–27), Saturday, October 24: rapid oral 1246RO (Rapid oral 2: Gynecological cancers, 8:30-10:00 CET) with first Phase 1 data for sofetabart mipitecan (Sofe-M), Lilly's investigational FRα-targeting ADC, plus bevacizumab in recurrent platinum-sensitive ovarian cancer; rapid oral 1RO (Rapid oral 1: Breast cancer, advanced stage, 10:15-11:45 CET) with overall survival from the Phase 3 postMONARCH trial of Verzenio (abemaciclib) plus fulvestrant vs placebo plus fulvestrant in HR+, HER2– advanced breast cancer after progression on a prior CDK4/6 inhibitor and endocrine therapy.Confirmed datePrimary source
October 24, 2026$MAZEMaze Therapeutics, Inc.ASN Kidney Week oral presentation of updated detail from previously reported Phase 2 HORIZON MZE829 data in APOL1-mediated kidney disease, October 24 at 5:40-5:50 pm MT. This is a presentation of earlier-reported results, not a new topline readout.Confirmed datePrimary source
24 October 2026$PBLSPARABILIS MEDICINES INCConference presentation: zolucatetide · desmoid tumor (Phase 1/2). Company timing: October 24, 2026. Congress: ESMO Congress.Confirmed datePrimary source
Supporting source
2026-10-24$REGNRegeneron Pharmaceuticals, Inc.ESMO poster 2490P: final Phase 2 analysis of neoadjuvant cemiplimab in resectable stage II–IV cutaneous squamous cell carcinoma.Confirmed datePrimary source
2026-10-24$REGNRegeneron Pharmaceuticals, Inc.ESMO poster 2091P: long-term overall survival follow-up from Phase 1 in advanced melanoma.Confirmed datePrimary source
2026-10-24$VERAVERA THERAPEUTICS INCASN oral presentation of interim Phase 2 PIONEER results in adult IgA nephropathy and primary membranous nephropathy, 5:30–5:40 p.m. MDT. Narrows the prior Q4 window.Confirmed datePrimary source
25 October 2026$ANABANAPTYSBIO INCConference presentation: Jemperli (dostarlimab) · Untreated stage II/III dMMR/MSI-H locally advanced rectal cancer AZUR-1 (pivotal Phase 2). Company timing: October 25, 2026. Congress: ESMO Congress.Confirmed datePrimary source
Supporting source
ANAB stock hub
2026-10-25$GRALGRAIL, Inc.ESMO poster 1164P on diagnostic workups after positive MCED blood tests in clinical practice is scheduled October 25, 12:00–12:45 conference local time.Confirmed datePrimary source
2026-10-25$GSKGSK / AnaptysBioESMO Congress 2026 (Madrid), Sunday, October 25, 10:15-11:45 CET, Proffered Paper Session: LBA87 (A. Cercek), "Clinical complete response with dostarlimab monotherapy in dMMR/MSI-H locally advanced rectal cancer (LARC): First results from the global registrational AZUR-1 trial" (Jemperli). This conference presentation is separate from the FDA review of Jemperli in rectal cancer. Sources: https://www.gsk.com/en-gb/media/press-releases/gsk-showcases-pipeline-momentum-across-lung-gynaecological-and-gastrointestinal-cancers-at-esmo-2026/ | https://www.sec.gov/Archives/edgar/data/1370053/000119312526396690/anab-ex99_1.htmConfirmed datePrimary source
SEC filing
2026-10-25$INBXINHIBRX BIOSCIENCES INCESMO Congress 2026 (Madrid), Sunday, October 25, 2026, 8:30-10:00 AM CET: oral presentation (lead author Jong Chul Park) of the phase 2 primary analysis of HexAgon-HN, a phase 2/3 study of the hexavalent OX40 agonist ordastobart (INBRX-106) in combination with pembrolizumab as first-line treatment of PD-L1-high recurrent/metastatic head and neck squamous cell carcinoma (R/M HNSCC).Confirmed datePrimary source
2026-10-25$INCYINCYTEESMO Congress 2026 (Madrid) rapid oral 1007RO, Sunday, October 25, 3:30-5:00 a.m. ET (8:30-10:00 a.m. CET): safety and efficacy of the oral KRAS G12D inhibitor INCB161734 as monotherapy or with cetuximab in advanced/metastatic colorectal cancer.Confirmed datePrimary source
2026-10-25$LLYEli Lilly and CompanyESMO Congress 2026 (Madrid), Sunday, October 25, 8:30-10:00 CET: rapid oral 2652RO (Rapid oral 2: NSCLC, metastatic) with updated integrated results from the Phase 1/2 LOXO-RAS-20001 trial and the safety lead-in of the Phase 3 SUNRAY-01 trial of olomorasib, Lilly's investigational KRAS G12C inhibitor, with chemoimmunotherapy (pembrolizumab, pemetrexed and platinum) as first-line treatment of advanced/metastatic KRAS G12C-mutant NSCLC.Confirmed datePrimary source
2026-10-25$MYGNMyriad Genetics, Inc.ESMO Congress 2026, Sunday, October 25, 2026: MONSTAR-SCREEN-3 data on the whole-genome-sequencing-based Precise MRD assay. Proffered paper on ultrasensitive ctDNA detection for molecular residual disease assessment in resectable colorectal cancer (Proffered Paper 1: Basic Science and Translational Research, Burgos Auditorium – Hall 3, 2:45-4:15 p.m.) and poster 3138P on MRD detection in resectable pancreatic cancer (12:00-12:45 p.m.).Confirmed datePrimary source
2026-10-25$REGNRegeneron Pharmaceuticals, Inc.ESMO late-breaking Phase 3 C-POST overall survival update at approximately 3.5 years in adjuvant high-risk cutaneous squamous cell carcinoma.Confirmed datePrimary source
2026-10-25$SMMTSummit Therapeutics Inc.ESMO 2026 (Madrid) oral presentation, Proffered Paper 2 Session: Genitourinary Tumours, Renal and Urothelial, October 25, 9:32-9:42 a.m. CET, Abstract #3592O: efficacy and safety of ivonescimab (AK112) as first-line treatment for IMDC favorable-risk advanced renal cell carcinoma, results from a Phase Ib/II investigator-sponsored study.Confirmed datePrimary source
2026-10-25$SMMTSummit Therapeutics / AkesoHARMONi-GI1 Phase 3 biliary-tract cancer presentation, ESMO Presidential Symposium II, Abstract LBA8, October 25, 5:42-5:54 p.m. CET (session 16:30-18:15 CET / 11:30-13:15 EDT). The company describes positive overall survival findings; Akeso-sponsored study conducted in China, with all relevant data generated, managed and analyzed by Akeso. Separate from the November 14 NSCLC PDUFA.Confirmed datePrimary source
Supporting source
2026-10-25$TNGXTANGO THERAPEUTICS INCESMO Congress 2026 (Madrid, October 23-27), Sunday, October 25, 12:00-12:45 pm CEST: poster 3149P (presenter Alexander I. Spira, MD, PhD, FACP, NEXT Oncology) with updated data from the Phase 1/2 study of vopimetostat in combination with daraxonrasib or zoldonrasib in patients with MTAP-deleted, RAS-mutant (MTAPdel/RASmut) metastatic pancreatic ductal adenocarcinoma (PDAC) and non-small cell lung cancer (NSCLC). The abstract data cutoff is April 3, 2026; the poster will include updated data.Confirmed datePrimary source
2026-10-26$EIKNEikon Therapeutics, Inc.ESMO Congress 2026 (Madrid) posters on Monday, October 26, 2026, 12:00 – 12:45: 2664P, TeLuRide-005 Phase 2 study of the TLR7/8 dual agonist EIK1001 plus pembrolizumab and chemotherapy in stage IV NSCLC, with results from the squamous cohort and updated pooled results; 2724TiP, design of the Phase 2/3 TeLuRide-008 trial of EIK1001 with pembrolizumab and chemotherapy in stage 4 NSCLC. Full-text abstracts published October 18.Confirmed datePrimary source
2026-10-26$GRALGRAIL, Inc.PATHFINDER 2 cancer-signal-origin-guided diagnostic workups, abstract 1151, scheduled within the October 26 ESMO rapid-oral session 14:45–16:15. This is a session window, not a confirmed individual talk time.Confirmed datePrimary source
2026-10-26$GSKGSK plcESMO Congress 2026 (Madrid), Monday, October 26: Rapid Oral Session 8:35-10:00 CET, 3718RO (S. Bauer), molecular response in KIT circulating tumour DNA from StrateGIST 1, Phase 1/1b study of velzatinib (IDRX-42) in advanced gastrointestinal stromal tumours; Poster Session 12:00-12:45 CET, 3841P (H. R. Kim), EMBOLD PanTumor-101 Ris-Rez dose optimisation in extensive-stage small cell lung cancer; Presidential Symposium 16:30-18:15 CET, LBA9 (L. Xie), late-breaking data presented by GSK's licensor Hansoh Pharma: primary results from the Phase 3 ARTEMIS-011 study of Ris-Rez versus gemcitabine and docetaxel in heavily pretreated relapsed or refractory osteosarcoma.Confirmed datePrimary source
2026-10-26$INCYINCYTEESMO Congress 2026 (Madrid) rapid oral 3137RO, Monday, October 26, 9:45-11:15 a.m. ET (2:45-4:15 p.m. CET): safety and efficacy of INCB161734, an oral KRAS G12D inhibitor, with chemotherapy in advanced/metastatic pancreatic ductal adenocarcinoma. The same day, from 2:30 to 4:00 p.m. ET, Incyte hosts an investor event and webcast to discuss key data presented at ESMO and provide portfolio updates.Confirmed datePrimary source
2026-10-26$IOVAIOVANCE BIOTHERAPEUTICS INCESMO Congress 2026: rapid oral presentation (abstract 3725RO) of lifileucel in previously treated undifferentiated pleomorphic sarcoma (UPS) or dedifferentiated liposarcoma (DDLPS), Monday, October 26, 2026, 08:30–10:00 CEST. Data from a pilot trial led by Memorial Sloan Kettering Cancer Center and supported by Iovance; the registrational SARATOGA trial in UPS and DDLPS is ongoing.Confirmed datePrimary source
SEC filing
2026-10-26$LLYEli Lilly and CompanyESMO Congress 2026 (Madrid), Monday, October 26, 10:15-11:45 CET: proffered paper 4208O (NETs and endocrine tumors) with updated results of the randomized Phase 3 LIBRETTO-531 study of Retevmo (selpercatinib) vs cabozantinib or vandetanib in advanced, kinase inhibitor-naïve, RET-mutant medullary thyroid cancer. The same day, 12:00-12:45, posters 1288P (Sofe-M in patients aged 65 or older with platinum-resistant and -sensitive ovarian cancer) and 2683P (first-line olomorasib plus pembrolizumab in KRAS G12C-mutant NSCLC).Confirmed datePrimary source
2026-10-26$REGNRegeneron Pharmaceuticals, Inc.ESMO Phase 2 ROXI-CATH subanalysis of catheter-related venous thromboembolism in patients with active cancer.Confirmed datePrimary source
2026-10-26$SMMTSummit Therapeutics Inc.ESMO 2026 (Madrid) rapid oral presentation, Rapid Oral Session: Non-metastatic NSCLC and Other Thoracic Malignancies, October 26, 11:07-11:12 a.m. CET, Abstract #4156RO: ivonescimab plus chemotherapy as first-line treatment in recurrent/metastatic thymic carcinoma, results from the iTHYM Phase II investigator-sponsored study.Confirmed datePrimary source
26 October 2026$ZLABZAI LAB LTDESMO poster 3817P (abstract 1569): zocilurtatug pelitecan (zoci), ZL1310-001 phase 1 parts 1b/1c, with atezolizumab with or without carboplatin in first-line extensive-stage SCLC. Poster date: October 26, 2026. Company release lists 12:00–12:45 CEST; timezone label is reproduced as published, not converted. ESMO congress runs October 23–27 in Madrid.Confirmed datePrimary source
ZLAB stock hub
2026-10-27$NAUTNautilus Biotechnology, Inc.Third-quarter 2026 financial results before market open on Tuesday, October 27, 2026, followed by a webcast conference call at 8:30 a.m. ET (5:30 a.m. PT).Confirmed datePrimary source
2026-10-27$PHARPharming Group N.V.Full preliminary third-quarter 2026 financial results and business update on October 27, 2026, brought forward from November 5, followed by a conference call and webcast at 13:30 CET / 8:30 a.m. EDT. Preliminary figures released October 22: total revenues of approximately $117.6 million, up about 21% year over year.Confirmed datePrimary source
2026-10-27$PROKProKidney Corp.Virtual key opinion leader event on Tuesday, October 27, 2026, at 10:30 a.m. ET: new insights into rilparencel's mechanism of action from research presented at ASN Kidney Week 2026, the potential role of rilparencel in advanced stage 3b/4 CKD with type 2 diabetes, a corporate update and a live Q&A.Confirmed datePrimary source
2026-10-28$AMRNAmarin Corporation plcThird-quarter 2026 financial results released in the pre-market hours of Wednesday, October 28, 2026, followed by a conference call with senior management at 8:00 a.m. ET.Confirmed dateFinviz (news)
2026-10-28$BEAMBeam Therapeutics Inc.ESGCT 33rd Annual Congress (Hamburg): poster with initial Phase 1/2 data for BEAM-301 in glycogen storage disease type Ia on October 28, 2026 (Poster Session I, P0219). Beam will review the data on an investor webcast on October 27 at 8:00 a.m. ET.Confirmed datePrimary source
2026-10-28$PYPDPolyPid Ltd.Virtual Investor Day "PolyPid 2030" on Wednesday, October 28, 2026, at 11:30 a.m. ET: management to outline its long-term growth and pipeline strategy, provide an update on D-PLEX (NDA under FDA Priority Review, PDUFA goal date November 28, 2026) and introduce PD01B, a new product candidate based on the Kynatrix delivery technology being developed for the treatment of diabetic foot infections.Confirmed datePrimary source
2026-10-28$REPLReplimune Group, Inc.Conference call on Wednesday, October 28, 2026, at 8:00 a.m. ET to discuss financial results and provide a corporate update for the fiscal second quarter ended September 30, 2026.Confirmed datePrimary source
2026-10-28$VKTXViking Therapeutics, Inc.Third-quarter 2026 financial results released after the market close on Wednesday, October 28, 2026, followed by a conference call on financial results and general corporate updates at 4:30 p.m. ET.Confirmed datePrimary source
2026-10-28$VNDAVanda Pharmaceuticals Inc.Third-quarter 2026 financial results to be released after the market close on Wednesday, October 28, 2026, followed by a conference call at 4:30 p.m. ET.Confirmed datePrimary source
2026-10-29$BBIOBridgeBio Pharma, Inc.Third-quarter 2026 financial results and business update released after the market closes on Thursday, October 29, 2026, followed by a conference call on financial results and program updates at 4:30 p.m. ET the same day.Confirmed datePrimary source
2026-10-29$INBXINHIBRX BIOSCIENCES INC2026 Musculoskeletal Tumor Society (MSTS) Annual Meeting (Miami, Florida), Thursday, October 29, 2026, 2:50-3:40 PM EST: oral presentation (lead author Robin Jones) of secondary efficacy endpoints from the randomized, registrational, Phase 2 ChonDRAgon study of the tetravalent death receptor 5 (DR5) agonist ozekibart (INBRX-109) in conventional chondrosarcoma.Confirmed datePrimary source
2026-10-29$LENZLENZ Therapeutics, Inc.Webcast on Thursday, October 29, 2026, at 8:30 a.m. EDT to report third-quarter 2026 financial results.Confirmed datePrimary source
2026-10-29$STOKStoke Therapeutics, Inc.Webcast and conference call for analysts and investors on Thursday, October 29, 2026, at 4:30 p.m. ET to discuss third-quarter 2026 business and financial updates.Confirmed dateFinviz (news)
2026-11-02$KRYSKRYSTAL BIOTECH INCThird-quarter 2026 financial results on Monday, November 2, 2026, before the U.S. market opens, followed by a conference call and webcast at 8:30 a.m. ET with a business update.Confirmed datePrimary source
2 November 2026$RXRXRECURSION PHARMACEUTICALS INCConference presentation: REC-4881 · Familial adenomatous polyposis. Company timing: 2 November 2026. Congress: CGA-IGC Annual Meeting.Confirmed datePrimary source
Supporting source
2026-11-03$ALKSALKERMES PLCThird-quarter 2026 financial results discussed on a conference call and webcast at 8:00 a.m. ET (1:00 p.m. GMT) on Tuesday, November 3, 2026.Confirmed dateFinviz (news)
2026-11-03$ARDXArdelyx, Inc.Third-quarter 2026 financial results and business update on a webcast and conference call on Tuesday, November 3, 2026, at 4:30 p.m. ET.Confirmed datePrimary source
2026-11-03$MDGLMadrigal Pharmaceuticals, Inc.Third-quarter 2026 financial results before the open of the U.S. financial markets on Tuesday, November 3, 2026, followed by a live webcast at 8:00 a.m. ET.Confirmed datePrimary source
2026-11-03$ZVRAZevra Therapeutics, Inc.Third-quarter 2026 corporate and financial results via news release after the market close on Tuesday, November 3, 2026, followed by a conference call and audio webcast at 4:30 p.m. ET.Confirmed datePrimary source
2026-11-04$ARQTArcutis Biotherapeutics, Inc.Third-quarter 2026 financial results and business update released after the U.S. financial markets close on Wednesday, November 4, 2026, followed by a conference call and webcast at 4:30 p.m. ET.Confirmed dateFinviz (news)
2026-11-04$BCRXBioCryst Pharmaceuticals, Inc.Third-quarter 2026 financial results reported on Wednesday, November 4, 2026, with a conference call and webcast at 8:30 a.m. ET that day to discuss the financial results and provide a corporate update.Confirmed datePrimary source
2026-11-04$BLLNBillionToOne, Inc.Third-quarter 2026 financial results after the market close on Wednesday, November 4, 2026, followed by a conference call at 1:30 p.m. PT / 4:30 p.m. ET the same day, with a live and archived webcast.Confirmed datePrimary source
Supporting source
2026-11-04$CYTKCYTOKINETICS INCThird-quarter 2026 results reported on Wednesday, November 4, 2026 at 4:00 p.m. ET, followed by a conference call by senior management at 4:30 p.m. ET to discuss financial results and provide business updates.Confirmed datePrimary source
2026-11-04$GERNGeron CorporationThird-quarter 2026 financial results and business highlights before the market opens on Wednesday, November 4, 2026, followed by a conference call and webcast at 8:00 a.m. ET.Confirmed dateFinviz (news)
2026-11-04$GRALGRAIL, Inc.Third-quarter 2026 financial results released following the close of market on Wednesday, November 4, 2026, followed by a webcast and conference call at 1:30 p.m. PT / 4:30 p.m. ET on results and business progress.Confirmed datePrimary source
2026-11-04$OCGNOcugen, Inc.Conference call and live webcast on Wednesday, November 4, 2026 at 8:30 a.m. ET to provide a business update and report third-quarter 2026 financial results.Confirmed datePrimary source
2026-11-04$SMMTSummit Therapeutics Inc.Virtual special meeting of stockholders on Wednesday, November 4, 2026, at 11:00 a.m. ET, to vote on an amendment to the Restated Certificate of Incorporation increasing authorized common stock by 1,000,000,000 shares (from 1,000,000,000 to 2,000,000,000). Record date: close of business October 1, 2026.Confirmed dateSEC filing
2026-11-04$STIMNeuronetics, Inc.Third-quarter 2026 financial and operating results released prior to market open on Wednesday, November 4, 2026, followed by a conference call and webcast at 8:30 a.m. ET.Confirmed dateFinviz (news)
2026-11-04$VIRVir Biotechnology, Inc.Conference call at 4:30 p.m. ET / 1:30 p.m. PT on Wednesday, November 4, 2026 to provide a corporate update and discuss financial results for the third quarter ended September 30, 2026.Confirmed datePrimary source
2026-11-04$VRDNVIRIDIAN THERAPEUTICS INCThird-quarter 2026 financial results before the market opens on Wednesday, November 4, 2026, followed by a live conference call at 8:00 a.m. ET with a business update.Confirmed dateFinviz (news)
2026-11-05$AGIOAgios Pharmaceuticals, Inc.Third-quarter 2026 financial results and business highlights on a conference call and live webcast on Thursday, November 5, 2026, at 8:00 a.m. ET.Confirmed datePrimary source
2026-11-05$CATXPerspective Therapeutics, Inc.NANETS oral abstract 36595: cohort 1–3 safety and efficacy in advanced SSTR2-positive neuroendocrine tumors. Issuer lists November 5 within the 4:10–5:25 p.m. PST session; no individual talk time is supplied.Confirmed datePrimary source
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Trial registry
Supporting source
2026-11-05$IVAInventiva S.A.AASLD poster 1052: plasma cell-free DNA methylation across PPAR isoforms in MASLD. Mechanistic/translational research; not the NATiV3 Phase 3 topline.Confirmed datePrimary source
2026-11-05$NYXHNyxoah SAThird-quarter 2026 financial results on November 5, 2026, with a webcast, as listed in the company investor events calendar.Confirmed datePrimary source
2026-11-05$RNXTRenovoRxThird-quarter 2026 financial results and business highlights released after market close on Thursday, November 5, 2026, followed by a conference call and webcast at 4:30 p.m. ET.Confirmed datePrimary source
2026-11-05$SRPTSarepta Therapeutics, Inc.Third-quarter 2026 financial results reported after the Nasdaq Global Market closes on Thursday, November 5, 2026, followed by a conference call at 4:30 p.m. ET to discuss the results.Confirmed datePrimary source
2026-11-05$VCELVericel CorporationThird-quarter 2026 financial results on Thursday, November 5, 2026, with a conference call and webcast at 8:30 a.m. ET on financial results and business highlights.Confirmed datePrimary source
2026-11-05$VERAVera Therapeutics, Inc.Third-quarter 2026 financial results and business updates on a live investor webcast on Thursday, November 5, 2026, at 4:30 p.m. ET.Confirmed datePrimary source
2026-11-05$VSTMVerastem, Inc.Conference call and webcast on Thursday, November 5, 2026, at 4:30 p.m. ET to discuss third-quarter 2026 financial results and business updates.Confirmed datePrimary source
2026-11-05$XERSXERIS BIOPHARMA HOLDINGS INCFinancial results and business highlights for the third quarter ended September 30, 2026 released before the open of the U.S. financial markets on Thursday, November 5, 2026, followed by a conference call and webcast at 8:30 a.m. ET that day.Confirmed datePrimary source
2026-11-05$ZLABZai Lab LimitedThird-quarter 2026 financial results and recent corporate updates on November 5, 2026, before the opening of U.S. equity markets, followed by a conference call and webcast at 8:00 a.m. ET (9:00 p.m. HKT).Confirmed datePrimary source
2026-11-06$CADLCandel Therapeutics, Inc.SITC poster 603: multi-omics and immune-activation analyses with aglatimagene plus valacyclovir in NSCLC progressing despite checkpoint inhibitors.Confirmed datePrimary source
2026-11-06$CATXPerspective Therapeutics, Inc.SITC poster 571: VMT01 mono- and combination therapy with nivolumab in previously treated unresectable or metastatic melanoma. Abstract details due November 3.Confirmed datePrimary source
Trial registry
2026-11-06$MRNAModerna, Inc.Moderna reports third-quarter 2026 financial results and provides a corporate update on Friday, November 6, 2026, with a webcast at 8:00 a.m. ET.Confirmed datePrimary source
2026-11-07$AGENAgenus Inc.SITC clinical poster 472: characteristics of long-term survivors with refractory MSS metastatic colorectal cancer treated with BOT+BAL.Confirmed datePrimary source
2026-11-07$CADLCandel Therapeutics, Inc.SITC poster 468: Phase 1b clinical and mechanistic findings for linoserpaturev combined with VEGF blockade in recurrent glioblastoma.Confirmed datePrimary source
2026-11-07$IVAInventiva S.A.AASLD posters 3552 and 3570: liver endothelial/vascular findings spanning preclinical models and Phase 2b analyses, plus preclinical hepatic-cell fibrosis mechanisms. Grouped same-day presentations; not NATiV3 results.Confirmed datePrimary source
November 8, 2026$CGEMCullinan Therapeutics, Inc.Velinotamig: multidose data from the Genrix Bio Phase 1 dose-escalation study in systemic lupus erythematosus, poster presentation at ACR Convergence on November 8, 2026, 10:30 a.m.–12:30 p.m. Eastern.Confirmed datePrimary source
2026-11-08$CRSPCRISPR Therapeutics AGACR poster 0225: Phase 1 safety and efficacy in refractory systemic sclerosis, November 8 at 10:30 a.m. ET. Specific subset presentation; broader H2 autoimmune/oncology guidance remains separate.Confirmed datePrimary source
2026-11-08$EDITEditas Medicine, Inc.AHA Scientific Sessions, November 8, 3:30–4:45 p.m. CT: preclinical durability of LDL-C reduction with EDIT-401 in non-human primates. Not human clinical data.Confirmed datePrimary source
2026-11-08$GILDGILEAD SCIENCES, INC.The Liver Meeting 2026 (AASLD, Denver, November 5-9): late-breaking oral presentation of Phase 3 IDEAL results on seladelpar for alkaline phosphatase normalization in primary biliary cholangitis (abstract #5007) on November 8, 2026. Gilead's program includes 21 accepted abstracts, among them a late-breaking fatigue poster on seladelpar (#5040, November 8), up-to-five-year seladelpar data and long-term and real-world Hepcludex (bulevirtide-gmod) data in chronic hepatitis delta.Confirmed dateFinviz (news)
8 November 2026$MLYSMINERALYS THERAPEUTICS INCTransform-HTN open-label extension: long-term efficacy and safety of lorundrostat in uncontrolled hypertension. Late-breaking AHA Scientific Sessions presentation on November 8 at 3:30 p.m. CT, Chicago. This is a clinical presentation, separate from the December PDUFA target. Company timing: November 8, 2026. Congress: AHA Scientific Sessions.Confirmed datePrimary source
Supporting source
MLYS stock hub
2026-11-09$ANTXAN2 Therapeutics, Inc.Guggenheim 3rd Annual Healthcare Innovation Conference (November 9–11, 2026): fireside chat with the CEO on Monday, November 9, 2026, at 9:30 a.m. ET, with a webcast. An investor conference appearance, not a data release.Confirmed dateFinviz (news)
November 9, 2026$ARTVArtiva Biotherapeutics, Inc.AlloNK (AB-101) plus rituximab updated Phase 2a basket data in refractory RA, Sjögren disease and systemic sclerosis at ACR 2026. Oral session November 9, 3:00-4:30 pm EST; investor webcast 8:15 am EST.Confirmed datePrimary source
November 9, 2026$CRSPCRISPR Therapeutics AGCTX310 Phase 1b results in severe hypertriglyceridemia: AHA late-breaking oral presentation November 9, 2026 at 8:00 a.m. CST. Data remain embargoed until presentation. Specifies the previously guided H2 2026 Phase 1b update; separate from Phase 1a ESC durability results.Confirmed datePrimary source
Supporting source
2026-11-09$GENBGENERATE BIOMEDICINES INCPresentation at the Guggenheim 3rd Annual Healthcare Innovation Conference in Boston on Monday, November 9, 2026, at 1:00 p.m. ET, with live webcast. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-09$IMVTIMMUNOVANT INCFinancial results for the second fiscal quarter ended September 30, 2026 reported on Monday, November 9, 2026 before the market opens. Roivant Sciences, Immunovant's majority stockholder, hosts a live conference call and webcast at 8:00 a.m. ET that day, including a business update for Immunovant.Confirmed datePrimary source
2026-11-09$LBRXLB Pharmaceuticals Inc.Guggenheim Securities 3rd Annual Healthcare Innovation Conference (Boston, MA): fireside chat at 1:00 p.m. ET and one-on-one investor meetings on Monday, November 9, 2026. Webcast on the company investor website. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-09$SENSSenseonics Holdings, Inc.Third-quarter 2026 financial results released after market close on Monday, November 9, 2026, followed by a conference call and webcast at 4:30 p.m. ET.Confirmed dateFinviz (news)
2026-11-09$ZYMEZymeworks Inc.Third-quarter 2026 financial results, after market close on November 9, 2026. No conference call or webcast planned.Confirmed datePrimary source
2026-11-10$ANTXAN2 Therapeutics, Inc.Stifel 2026 Healthcare Conference (November 10–12, 2026): corporate overview by the CEO on Tuesday, November 10, 2026, at 8:40 a.m. ET, with a webcast. An investor conference appearance, not a data release.Confirmed dateFinviz (news)
November 10, 2026$ARTVArtiva Biotherapeutics, Inc.AlloNK (AB-101) plus rituximab safety and B-cell depletion data from a 60-patient rheumatology cohort, ACR poster 2384 November 10, 10:30 am-12:30 pm EST. Separate poster from the November 9 oral efficacy update; overlapping patients are possible.Confirmed datePrimary source
2026-11-10$EPRXEupraxia Pharmaceuticals Inc.Eupraxia fireside chat at the Stifel 2026 Healthcare Conference (New York, November 10-12, 2026) on November 10, 2026, at 4:40 p.m. ET, with webcast and one-on-one meetings. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-10$IPHAInnate Pharma S.A.Innate Pharma will participate in a fireside chat at the Stifel Healthcare Conference (New York, November 10-12, 2026) on Tuesday, November 10, 2026, at 2:00 p.m. ET (8:00 p.m. CET), with a live webcast and a replay to follow. Members of the executive team will represent the company; an investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-10$SENSSenseonics Holdings, Inc.Senseonics fireside chat at the Stifel 2026 Healthcare Conference (New York, November 10-12, 2026) on Tuesday, November 10, 2026, at 3:20 p.m. ET, with live webcast and one-on-one meetings. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-10$SRRKScholar Rock Holding CorporationThird-quarter 2026 financial results before the market open on Tuesday, November 10, 2026, followed by a conference call and webcast at 8:00 a.m. ET.Confirmed dateFinviz (news)
2026-11-10$TLSITriSalus Life Sciences, Inc.Third-quarter 2026 financial results: conference call and webcast on Tuesday, November 10, 2026, at 8:30 a.m. ET; a press release with the results will be issued before the call.Confirmed dateFinviz (news)
2026-11-11$SENSSenseonics Holdings, Inc.Senseonics presentation at the 20th Annual Canaccord Genuity MedTech, Diagnostics & Digital Health Forum (New York) on Wednesday, November 11, 2026, at 10:30 a.m. ET, with live webcast and one-on-one meetings. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-11$TEVATeva Pharmaceutical Industries Ltd.Teva R&D Day in New York on November 11, 2026, 8:30 a.m. to 12:30 p.m. ET: leadership to discuss the R&D pipeline and near-term value-creation potential over the next five years. Live webcast on the investor relations site.Confirmed datePrimary source
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2026-11-12$LBRXLB Pharmaceuticals Inc.Stifel Healthcare Conference (New York, NY): fireside chat at 9:20 a.m. ET and one-on-one investor meetings on Thursday, November 12, 2026. Webcast on the company investor website. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-13$DRTSAlpha Tau Medical LTD.Society for Neuro-Oncology (SNO) 2026 Annual Meeting (Philadelphia), Friday, November 13, 2026, 7:30–9:30 p.m. ET: presentation of the safety interim analysis of REGAIN (NCT06910306), the U.S. study of Alpha DaRT in recurrent glioblastoma, including new trial data that build on the interim results announced on May 11, 2026 from the first three treated patients.Confirmed dateSEC filing
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2026-11-13$EPRXEupraxia Pharmaceuticals Inc.Virtual Analyst Day to discuss EP-104GI for eosinophilic esophagitis on November 13, 2026, at 8:30 a.m. ET, with webcast.Confirmed datePrimary source
2026-11-13$ZLABZai Lab LimitedACAAI 2026 (Phoenix): first clinical data for ZL-1503, an IL-13/IL-31R bispecific antibody, from the healthy-volunteer study NCT07235384 as ePoster R376 on November 13, 2026 at 2:50 p.m. MT (4:50 p.m. ET); Zai Lab conference call the same day at 8:00 a.m. ET. Healthy-volunteer pharmacokinetics, biomarkers and initial safety, not patient efficacy.Confirmed datePrimary source
2026-11-15$AMLXAmylyx Pharmaceuticals, Inc.ObesityWeek presentation of Phase 3 LUCIDITY in post-bariatric hypoglycemia, 08:30–08:45 ET. Topline was previously announced in August; this is the scientific presentation.Confirmed datePrimary source
2026-11-15$CRBPCorbus Pharmaceuticals Holdings, Inc.Late-breaking poster at ObesityWeek 2026 (National Harbor, MD, November 14-17): efficacy, safety and tolerability of CRB-913 in the Phase 1b CANYON-1 study, November 15, 2026, 2:30-3:30 p.m. ET, Gaylord National Resort & Convention Center, Exhibit Hall BCD.Confirmed datePrimary source
2026-11-15$GPCRStructure Therapeutics Inc.Conference presentation: aleniglipron (oral small-molecule GLP-1 receptor agonist) · overweight and obesity. Two posters at ObesityWeek 2026 (National Harbor, MD, November 14-17): ACCESS trial open-label extension, and dose-ranging effects across the ACCESS trials. Both on November 15, 2026, 2:30-3:30 p.m. ET. Congress: ObesityWeek 2026.Confirmed datePrimary source
2026-11-16$EPRXEupraxia Pharmaceuticals Inc.Eupraxia presentation at the 2026 Jefferies Global Healthcare Conference in London (November 16-19, 2026) on November 16, 2026, at 1:30 p.m. GMT, with webcast and one-on-one meetings. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-16$GENBGENERATE BIOMEDICINES INCPresentation at the Jefferies Global Healthcare Conference in London on Monday, November 16, 2026, at 10:30 a.m. ET, with live webcast. An investor conference appearance, not a data release.Confirmed datePrimary source
2026-11-19$ANVSAnnovis Bio, Inc.CTAD 2026 (Boston, November 16-19): oral communication on buntanetap in Alzheimer's disease, Biotech Showcase 7, November 19, 2026, 3:52 p.m. ET. Two posters are on display November 16, 2:00 p.m. to November 17, 5:30 p.m. ET: P025 on the trial design and baseline characteristics of the pivotal Phase 3 study in early Alzheimer's disease, and P121 on AI-based prediction of blood-brain barrier permeability. The company expects the pivotal data readout in early 2027.Confirmed datePrimary source
2026-11-19$INBXINHIBRX BIOSCIENCES INC2026 Connective Tissue Oncology Society (CTOS) Annual Meeting (Seoul, South Korea), Thursday, November 19, 2026, 5:30-6:30 PM KST: poster presentation (lead author Varun Monga) of the Phase 1/2 study of the tetravalent death receptor 5 (DR5) agonist ozekibart (INBRX-109) combined with irinotecan and temozolomide in adolescents and adults with Ewing sarcoma.Confirmed datePrimary source
2026-11-20$INBXINHIBRX BIOSCIENCES INC2026 Connective Tissue Oncology Society (CTOS) Annual Meeting (Seoul, South Korea), Friday, November 20, 2026, 11:00 AM-12:30 PM KST: oral presentation (lead author Sant Chawla) of subgroup analysis and updated progression-free survival (PFS) from the randomized, Phase 2 ChonDRAgon study of the tetravalent death receptor 5 agonist ozekibart (INBRX-109) in conventional chondrosarcoma.Confirmed datePrimary source
2026-12-08$OCSOculis Holding AGOculis R&D Day on December 8, 2026, with updates on the late-stage pipeline, including privosegtor and licaminlimab.Confirmed datePrimary source
2026-12-14$MBOTMicrobot Medical Inc.2026 annual meeting of stockholders on Monday, December 14, 2026, set by the Board of Directors on October 14, 2026. Record date: October 15, 2026. The exact time and location will be specified in the proxy statement for the meeting.Confirmed dateSEC filing
2026-12-22$OCGNOcugen, Inc.Postponed special meeting of stockholders on the proposal to increase authorized common stock by 250,000,000 shares: Tuesday, December 22, 2026, 8:00 a.m. ET, virtual. Record date: close of business October 30, 2026. The meeting had previously been adjourned to October 26, 2026; the board postponed it on October 14, 2026.Confirmed dateSEC filing

Conferences with a confirmed range: 20 events

The range refers to the conference dates. Any confirmed individual presentation day is stated in the row; other presentation days are not inferred from the conference start.

Date / windowTickerCompanyEventStatusSources
October 22–23, 2026$CLYMClimb Bio, Inc.ASN CLYM116 Phase 1 poster October 22 and MIL116 preliminary Phase 1 healthy-volunteer poster October 23. Refines the prior Q4 clinical-data package.Conference rangePrimary source
October 21–23, 2026; ePoster day unspecified$ZBIOZenas BioPharma, Inc.MSToronto ePoster EP2593: pharmacokinetic analysis from the Phase 2 RRMS study. Distinct from the October 22 efficacy poster; no exact ePoster day is disclosed.Conference rangePrimary source
Supporting source
October 21–25, 2026$MLYSMineralys Therapeutics, Inc.ASN Launch-HTN analysis of blood pressure and albuminuria in CKD stages 1–3. Conference window October 21–25; individual presentation day not provided in the company release.Conference rangePrimary source
MLYS stock hub
October 21–25, 2026$TVTXTravere Therapeutics, Inc.ASN Kidney Week package includes SPARTAN two-year IgAN data, post hoc DUPLEX FSGS analysis and PROTECT biomarker analyses. Conference dates are a package window, not the time of one session; results described in the October 2 release.Conference rangePrimary source
ESMO Congress 2026-10-23–2026-10-27$BHVNBIOHAVEN LTDConference presentation: BHV-1530 · Advanced solid tumors (Phase 1). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$GENBGENERATE BIOMEDICINES INCConference presentation: GB-4362 · locally advanced or metastatic urothelial cancer (Phase 1). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$HCMHUTCHMED (CHINA) LTDConference presentation: ORPATHYS (savolitinib) plus TAGRISSO (osimertinib). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$HCMHUTCHMED (CHINA) LTDSANOVO Phase III savolitinib plus osimertinib results selected for an oral Proffered Paper presentation at ESMO. Separate from the SAFFRON Presidential Symposium presentation. Company timing: ESMO Congress, October 23–27, 2026. The congress dates do not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$IDYAIDEAYA BIOSCIENCES INCConference presentation: IDE849 (DLL3 TOP1i ADC) · small-cell lung cancer (SCLC) and neuroendocrine carcinomas (NEC) (Phase 1). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$IDYAIDEAYA BIOSCIENCES INCConference presentation: darovasertib combination (Phase 2). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$IDYAIDEAYA BIOSCIENCES INCConference presentation: darovasertib · Primary uveal melanoma; Metastatic uveal melanoma. Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$ONCYOncolytics Biotech Inc.ESMO Congress 2026 (October 23–27, 2026): trial-in-progress e-poster (presentation number 994eTiP) on REO 033, a randomized Phase 2 study of pelareorep plus FOLFIRI and bevacizumab versus FOLFIRI and bevacizumab alone as second-line treatment for RAS-mutated, microsatellite-stable metastatic colorectal cancer (30 patients per arm; primary endpoint objective response rate). The company has not announced the day of the e-poster within the congress dates.Conference rangeSEC filing
SEC filing
Supporting source
ESMO Congress 2026-10-23–2026-10-27$ORICORIC PHARMACEUTICALS INCConference presentation: enozertinib · 1L NSCLC with EGFR atypical mutations. Company timing: ESMO Congress, October 23–27, 2026. The congress dates do not establish the individual presentation day.Conference rangePrimary source
Supporting source
ESMO Congress 2026-10-23–2026-10-27$XNCRXENCOR INCConference presentation: XmAb819 · Clear cell renal cell carcinoma (RCC) (Phase 1). Company timing: ESMO Congress, October 23–27, 2026. Congress: ESMO Congress. The conference range does not establish the individual presentation day.Conference rangePrimary source
Supporting source
CTAD 2026, Nov 16-17, 2026$ABOSAcumen Pharmaceuticals, Inc.Three posters at the 19th Clinical Trials on Alzheimer's Disease (CTAD) conference in Boston (November 16-19, 2026), Poster Session 1, Monday, November 16, 2:00 p.m. to Tuesday, November 17, 5:30 p.m. EST: P015 on baseline characteristics of participants randomized in the Phase 2 ALTITUDE-AD trial of sabirnetug in early Alzheimer's disease, and P023 and P024 on treatment expectations, trial participation and care-partner experiences. No new efficacy results are announced.Conference rangePrimary source
November 16-19, 2026 conference; presentation day unspecified$ACADAcadia Pharmaceuticals Inc.RADIANT Phase 2 remlifanserin detailed safety and efficacy oral presentation at CTAD, confirmed for the November 16–19, 2026 conference; the presentation day has not been specified. The primary endpoint was not statistically met.Conference rangePrimary source
Supporting source
Nov 16-19, 2026$IPHAInnate Pharma S.A.Innate Pharma will participate in the Jefferies Global Healthcare Conference (London, November 16-19, 2026); the company's press release does not specify the day, time, or format of its appearance. An investor conference appearance, not a data release.Conference rangePrimary source
Signed Oct 19, 2026; closing expected by Feb 19, 2027 (HSR clearance pending)$MYGNMyriad Genetics, Inc.Myriad Genetics signed an Asset Purchase Agreement, dated October 19, 2026, to sell its prenatal health business — the Foresight Carrier Screen, Prequel Prenatal Screen, FirstGene 4-in-1 Prenatal Screen (an LDT), and the SneakPeek Early Gender Test — to Laboratory Corporation of America Holdings (LabCorp), for $210 million in cash plus the value of the business's inventory at closing. LabCorp owes a $10.5 million termination fee under specified circumstances tied to regulatory approvals. The agreement's outside date is February 19, 2027, automatically extended to October 19, 2027 if only regulatory clearances (including under the Hart-Scott-Rodino Act) remain outstanding. Closing is also expected to include a patent license agreement with a LabCorp affiliate and a transition services agreement; LabCorp will offer employment to affected employees on comparable terms.Conference rangeSEC filing
Q1 2027$BHVNBiohaven Ltd.FDA accepted for review the resubmitted NDA for VYGLXIA (troriluzole) for spinocerebellar ataxia (SCA); the resubmission included new positive supportive analyses. The FDA considers it a complete response to the November 4, 2025 action letter and assigned a user fee goal date in the first quarter of 2027. The FDA plans to convene a meeting of the Peripheral and Central Nervous System Advisory Committee; the meeting date has not yet been announced. The PDUFA target action date is a goal and does not assure approval.Conference rangeSEC filing
Q1 2027$CRMDCorMedix TherapeuticsFDA accepts for Priority Review the supplemental NDA for REZZAYO (rezafungin for injection) for prophylaxis of invasive fungal disease in adults undergoing allogeneic hematopoietic stem cell transplantation, based on the Phase 3 ReSPECT trial. PDUFA target action date in Q1 2027. Partner: Mundipharma.Conference rangeSEC filing
SEC filing

Company windows and explicit estimates: 544 events

Quarters, half-years and other windows are company guidance, not exact dates. Estimates derived from a regulatory review duration are labeled as calculated. A window-end marker is not an announced readout day. Filings, study starts and results are different milestones.

Date / windowTickerCompanyEventStatusSources
October 2026$IVVDInvivyd, Inc.VYD2311 DECLARATION placebo-controlled safety and neutralizing-antiviral-titer topline expected in October 2026. Clinical efficacy events remain blinded and a BLA is only planned, subject to supportive data.Estimated windowPrimary source
October 2026$MIRMMirum Pharmaceuticals / IncyteAtebrioz US commercial launch expected October 2026; exact day not announced. Estimated window: October 2026.Estimated windowPrimary source
October 2026$TLSATiziana Life Sciences Ltd.INFORM-MS foralumab 12-week topline. Estimated window: October 2026. Exact event day is not announced.Estimated windowPrimary source
Around November 1, 2026 (calculated)$QUREuniQure N.V.AMT-130 BLA filing-review decision window. Estimated: around November 1, 2026 (calculated). November 1 is calculated from 60 calendar days after the September 2 submission; the issuer did not announce an exact decision day. Priority review was requested, not granted. This is not a PDUFA deadline.Estimated windowPrimary source
ACAAI Annual Scientific Meeting 2026-11-12–2026-11-16$ADMAADMA BIOLOGICS INCASCENIV real-world outcomes abstract submitted to ACAAI. Acceptance and an individual presentation date are not confirmed by the cited release. Company timing: ACAAI Annual Scientific Meeting, November 12–16, 2026. Exact event day is not announced. Congress: ACAAI Annual Scientific Meeting. The conference range does not establish the individual presentation day.Estimated windowPrimary source
Supporting source
17 October–16 November 2026$RAREUltragenyx Pharmaceutical Inc.FAYUVI commercial product expected available to ship to qualified treatment centers within 30-60 days of September 17 approval: October 17-November 16, 2026.Estimated windowPrimary source
September–November 2026$ACADACADIA PHARMACEUTICALS INCTopline data: DAYBUE (trofinetide) · Rett syndrome (RTT). Company timing: September–November 2026. Exact event day is not announced.Estimated windowPrimary source
November 2026$CRVOCervoMed Inc.CervoMed plans to present 24-week nfvPPA biomarker data at CTAD in November 2026. The October 12 release does not specify the presentation day.Estimated windowPrimary source
November 2026$IBRXIMMUNITYBIO, INC.QUILT-2.005 cohort A, registrational trial of ANKTIVA plus BCG versus BCG alone in BCG-naive non-muscle-invasive bladder cancer (366 patients randomized): database lock announced October 21, 2026; final analysis of the primary endpoint and key secondary endpoints underway, topline results expected in November 2026. Exact day not announced.Estimated windowPrimary source
November 2026$PHARPharming Group N.V.Leniolisib: topline Phase II results from the trial in CVID patients with immune dysregulation, with or without an identified genetic cause, expected in November 2026 according to the company. Pharming is working towards a single registrational Phase III trial in the broader CVID indication. Exact day not announced.Estimated windowPrimary source
November 2026$RHHBYRoche Holding AGGazyva/Gazyvaro (obinutuzumab): FDA decision window in primary membranous nephropathy. Estimated window: November 2026. Priority Review is confirmed, but the issuer states November, not a specific day.Estimated windowPrimary source
Late November 2026$SLGLSol-Gel Technologies Ltd.SGT-610 (patidegib gel 2%), pivotal Phase 3 in Gorlin syndrome. September 17 company update reports last patient last visit and expects topline results in late November 2026. Registry completion is a separate milestone.Estimated windowPrimary source
Early November 2026$SXTP60 Degrees Pharmaceuticals, Inc.Additional screening data from expanded access in refractory babesiosis expected early November 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2026$AAPGASCENTAGE PHARMA GROUP INTERNATIONALInitial data: APG-3288 (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ABCLABCELLERA BIOLOGICS INCTopline data: ABCL575 (Phase 1). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ABOSAcumen Pharmaceuticals, Inc.Topline results from ALTITUDE-AD (NCT06335173), the Phase 2 trial of sabirnetug administered every four weeks in early Alzheimer's disease, which enrolled 542 participants, expected in late 2026 according to the company. Exact day not announced.Estimated windowPrimary source
H2 2026$ABSIABSCI CORPInterim data: ABS-201 · PHL. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ABVXABIVAX SANDA/BLA submission: obefazimod · Ulcerative colitis (UC) (Phase 3). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$ADMAADMA BIOLOGICS INCFDA meeting: SG-001 · Streptococcus pneumoniae infection. Company timing: By year-end 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$AGIOAGIOS PHARMACEUTICALS INCTopline data: tebapivat · sickle cell disease (SCD) (Phase 2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$AGIOAGIOS PHARMACEUTICALS INCInitial data: AG-181 · Phenylketonuria (PKU) (Phase 1b). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ALKSALKERMES PLCNDA/BLA submission: LUMRYZ (sodium oxybate) · Idiopathic hypersomnia (Phase 3). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ALKSALKERMES PLCTopline data: alixorexton · Idiopathic hypersomnia (phase 2). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ALMSAlumis Inc.Envudeucitinib NDA for moderate-to-severe plaque psoriasis planned for Q4 2026. Company guidance; not yet a submitted or accepted filing. Exact event day is not announced.Estimated windowPrimary source
H2 2026$ALNYAlnylam Pharmaceuticals, Inc.ALN-6400 Phase 1/2 and ALN-2232 Phase 1 readouts expected H2 2026; October 1 is an indicative placement, not an announced clinical date.Estimated windowPrimary source
Late 2026$ALVOALVOTECHPotential regulatory decision (company forecast): Biologics License Applications. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
2026$ALVOALVOTECHRegulatory decision: relevant BLAs. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$AMLXAMYLYX PHARMACEUTICALS INCNDA/BLA submission: avexitide · Post-bariatric hypoglycemia. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$ARCTArcturus Therapeutics Holdings Inc.ARCT-2601 integration into the ongoing OTC-deficiency Phase 2 study. Estimated: by year-end 2026. Company plan following the September 23 ARCT-810 interim announcement; regulatory and operational execution remain prospective.Estimated windowPrimary source
Q4 2026$ARQTARCUTIS BIOTHERAPEUTICS INCClinical data readout: ZORYVE foam 0.3% · Vitiligo (Phase 2). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$ARWRARROWHEAD PHARMACEUTICALS INCPlozasiran sNDA for severe hypertriglyceridemia targeted by year-end 2026. Entry into the FDA STAR pilot was announced on October 7; this does not imply a completed submission, an acceptance or an FDA decision date. Exact event day is not announced.Estimated windowPrimary source
Supporting source
Q4 2026$ATAIATAIBECKLEY INCInitial data: BPL-003 · treatment-resistant depression (TRD) (Phase 2a). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ATAIATAIBECKLEY INCTopline data: VLS-01 · TRD (Phase 2). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$AVBPARRIVENT BIOPHARMA INCARR-217 Phase 1 dose-escalation completion and transition to dose optimization. No interim-results publication is promised by this milestone. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$AXSMAXSOME THERAPEUTICS INCTopline data: solriamfetol · Binge eating disorder ENGAGE (Phase 3). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$BBIOBridgeBio Pharma, Inc.Submission of the achondroplasia marketing authorization application to EMA planned Q4 2026; company guidance, not an EMA decision date. Exact event day is not announced.Estimated windowPrimary source
H2 2026$BCAXBICARA THERAPEUTICS INCInitial data: ficerafusp alfa · 3L+ mCRC (RAS/BRAF wild type MSS); mCRC (RAS/BRAF wild type MSS) (Phase 1b). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
by end of 2026$BCRXBioCryst Pharmaceuticals, Inc.BCX17725 Phase 1 Part 4 data in Netherton syndrome. Estimated: by end of 2026. Up to 12 patients followed for three months; no exact release day.Estimated windowPrimary source
2026$BEAMBEAM THERAPEUTICS INCFull data: BEAM-302 · Alpha-1 antitrypsin deficiency (AATD). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$BEAMBEAM THERAPEUTICS INCClinical data readout: ristoglogene autogetemcel (risto-cel) · sickle cell disease (SCD), BEACON (Phase 1/2). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$BHVNBIOHAVEN LTDTopline data: opakalim · Focal epilepsy (pivotal). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$BHVNBIOHAVEN LTDTopline data: taldefgrobep alfa · Obesity (Phase 2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$BIOABioAge Labs, Inc.QUELL-CV BGE-102 Phase 2 topline in cardiovascular risk. Estimated: H2 2026. Enrollment completed; timing guidance reaffirmed September 8. Exact event day is not announced.Estimated windowPrimary source
Supporting source
Q4 2026$CELCCELCUITY INCClinical data readout: REVTORPYK (gedatolisib) · Metastatic castration-resistant prostate cancer (Phase 2). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
December 2026$CGEMCullinan Therapeutics, Inc.CLN-049: updated Phase 1 dose-escalation data with longer follow-up in relapsed/refractory acute myeloid leukemia, expected in December 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$CGEMCullinan Therapeutics, Inc.Completion of first-line zipalertinib-plus-chemotherapy RTOR NDA submission expected by year-end 2026; filing completion, not FDA acceptance or approval. Exact event day is not announced.Estimated windowPrimary source
December 2026$CGEMCullinan Therapeutics, Inc.CLN-978: concurrent multidose and single-target-dose clinical data in systemic lupus erythematosus, rheumatoid arthritis and Sjögren's disease, expected in December 2026. One planned package across three indications. Exact event day is not announced.Estimated windowPrimary source
2026$CGONCG ONCOLOGY INCBOND-003 Cohort P durability data in high-risk BCG-unresponsive Ta/T1 non-muscle-invasive bladder cancer without carcinoma in situ. Cohort C and CORE-008 Cohort A data are represented separately. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$CGONCG ONCOLOGY INCNDA/BLA submission: cretostimogene · HR BCG-unresponsive NMIBC. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$CLDXCELLDEX THERAPEUTICS INCTopline data: barzolvolimab · Atopic dermatitis (AtD) (Phase 2). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
2026$COGTCOGENT BIOSCIENCES INCIND submission: CGT1145. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
COGT stock hub
2026$COGTCOGENT BIOSCIENCES INCInitial data: CGT4859 (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
COGT stock hub
2026$COGTCOGENT BIOSCIENCES INCIND submission: CGT1815 · Cancer. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
COGT stock hub
Late 2026$COGTCOGENT BIOSCIENCES INCPreliminary results from the SUMMIT extension cohort switching patients from avapritinib to bezuclastinib. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
COGT stock hub
H2 2026$CRSPCRISPR THERAPEUTICS AGClinical data readout: CTX611 (SRSD107) · Thromboembolic and clotting-related indications (Phase 2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$CRSPCRISPR THERAPEUTICS AGClinical data readout: zugocabtagene geleucel (zugo-cel; formerly CTX112™) · B-cell malignancies; systemic lupus erythematosus (SLE), systemic sclerosis, inflammatory myositis, immune thrombocytopenic purpura, and warm autoimmune hemolytic anemia (Phase 1/2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
2026$CRSPCRISPR THERAPEUTICS AGPreclinical program update: CTX321™ · elevated lipoprotein(a) [Lp(a)]. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$CRVOCervoMed Inc.First dosing with neflamapimod in EXPERTS-ALS Phase 2a is expected in Q4 2026. Company guidance; dosing has not been confirmed by this announcement.Estimated windowPrimary source
Q4 2026$CYTKCYTOKINETICS INCNDA/BLA submission: MYQORZO (aficamten) · symptomatic nHCM (Phase 3). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
2026$DFTXDEFINIUM THERAPEUTICS INCInitial data: MM402 (R(-)-MDMA) · Autism Spectrum Disorder (Phase 2a). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$DFTXDefinium TherapeuticsDT120 ODT — pre-NDA meeting scheduled in Q4 2026. December 31 is the conventional end of the October–December window, not the exact meeting date.Estimated windowPrimary source
H2 2026$DMRADAMORA THERAPEUTICS INCIND submission: DMR-002. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$DMRADAMORA THERAPEUTICS INCRegulatory submissions to expand the Phase 1/1b DMR-001 trial globally in essential thrombocythemia and myelofibrosis. These are trial authorizations, not marketing applications. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
December 2026$DNTHDIANTHUS THERAPEUTICS INCTopline data: claseprubart · Multifocal motor neuropathy (Phase 2). Company timing: December 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$DNTHDIANTHUS THERAPEUTICS INCInitial data: DNTH212 · systemic lupus erythematosus (SLE) (Phase 1). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$DRTSALPHA TAU MEDICAL LTDPMA submission: Alpha DaRT · cutaneous squamous cell carcinoma ReSTART. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026$DRTSALPHA TAU MEDICAL LTDInterim data: Alpha DaRT · REGAIN, recurrent glioblastoma. Company timing: Late 2026 (last stated August 10, 2026: additional data expected around the end of 2026). On October 19, 2026 the company announced that the FDA approved an expansion of REGAIN from 10 to 20 patients and a protocol provision for an additional interim analysis six months after the fifth patient's treatment, which occurred in July 2026; no release date for that analysis was given. Exact event day is not announced.Estimated windowSEC filing
SEC filing
By year-end 2026$EDITEditas Medicine, Inc.Editas expects to begin dosing EDIT-401 in the Phase 1/2 Strive HeFH trial by year-end 2026. Company guidance; no exact event day announced.Estimated windowPrimary source
Q4 2026$ELDNEledon Pharmaceuticals, Inc.LEGACY Phase 3 kidney-transplant trial initiation. Estimated window: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$ELVNEnliven Therapeutics, Inc.Enliven says ENABLE-2 Phase 3 of relcobatinib (ELVN-001) in previously treated CML remains on track to initiate before year-end 2026 after FDA alignment on the trial design. Exact start day is not announced.Estimated windowPrimary source
December 2026$EPRXEupraxia Pharmaceuticals Inc.RESOLVE Phase 2b interim data for EP-104GI in eosinophilic esophagitis expected in December 2026. Company guidance; no exact day announced. Separate from open-label Phase 1b/2a data being presented in October.Estimated windowPrimary source
H2 2026$ERASERASCA INCInitial data: ERAS-4001 · RAS-mutant solid tumors (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$ETONETON PHARMACEUTICALS INCTopline data: ET-700 · Wilson disease. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ETONETON PHARMACEUTICALS INCNDA/BLA submission: AMGLIDIA®. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$EWTXEDGEWISE THERAPEUTICS INCGRAND CANYON pivotal cohort topline results in Becker muscular dystrophy. Servier acquired sevasemten and the muscular-dystrophy business in July 2026; Edgewise retains exposure through contingent milestone payments. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
later in 2026$GOSSGossamer Bio, Inc.FDA filing-acceptance review of seralutinib NDA. Estimated: later in 2026. The company expects this could occur later this year. No PDUFA date has been announced, and the timing is not guaranteed for Q4.Estimated windowPrimary source
Q4 2026$GPCRSTRUCTURE THERAPEUTICS INCResults from the Phase 2 aleniglipron study in adults with type 2 diabetes and obesity or overweight. Separate from the 44-week body-composition study. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q4 2026$GPCRSTRUCTURE THERAPEUTICS INCResults from the 44-week Phase 2 body-composition trial of aleniglipron, evaluating body fat and overall body composition. This is separate from the Phase 2 diabetes study. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q4 2026$GRFSGRIFOLS SATopline data: alpha-1 antitrypsin · Emphysema SPARTA (Phase 3). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$HCMHUTCHMED (CHINA) LTDClinical trial initiation: HMPL-A830 · Solid tumors. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
2026$HCMHUTCHMED (CHINA) LTDIND submission: ATTC candidates. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$HELPCybin Inc. doing business as Helus PharmaHLP003 APPROACH Phase 3 pivotal study (adjunctive treatment of major depressive disorder, 223 participants enrolled): topline data readout on track for Q4 2026, as reiterated at the October 21, 2026 investor presentation. Exact day not announced.Estimated windowPrimary source
Q4 2026$HRMYHARMONY BIOSCIENCES HOLDINGS INCTopline data: BP-205 (Phase 1). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$HROWHARROW INCTopline data: NATACYN · fungal keratitis. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$HROWHARROW INCTopline data: IHEEZO · patients undergoing intravitreal injections QUELL (Phase 4). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$HUMAHumacyte, Inc.Humacyte targets an FDA supplemental BLA for arteriovenous access for hemodialysis in Q4 2026. This is a planned submission, separate from the existing vascular-trauma approval.Estimated windowCompany release
Q4 2026$IBRXIMMUNITYBIO, INC.Planned sBLA submission to the FDA for ANKTIVA plus BCG in BCG-naive non-muscle-invasive bladder cancer, based on QUILT-2.005; the company said on October 21, 2026 that it remains on track for the fourth quarter of 2026. Exact day not announced.Estimated windowPrimary source
H2 2026$IDYAIDEAYA BIOSCIENCES INCNDA/BLA submission: darovasertib in combination with crizotinib · Metastatic uveal melanoma (registrational). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
2026$IDYAIDEAYA BIOSCIENCES INCConference presentation: IDE397 · MTAP-deleted urothelial cancer (UC) (Phase 1/2). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$IMCRIMMUNOCORE HOLDINGS PLCTopline data: KIMMTRAK (tebentafusp) · previously treated advanced melanoma. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IMCRIMMUNOCORE HOLDINGS PLCIND submission: IMC-U120AI · atopic dermatitis (AtD); autoimmune candidate. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IMCRIMMUNOCORE HOLDINGS PLCConference presentation: IMC-P115C · solid tumors; Multiple solid tumors (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IMCRIMMUNOCORE HOLDINGS PLCConference presentation: brenetafusp · solid tumors; ovarian and lung cancer (Phase 1/2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$IMNMIMMUNOME INCIND submission: IM-1335. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
2026$IMNMIMMUNOME INCIND submission: solid tumor-targeted ADC programs · Solid tumors. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
2026$IMNMIMMUNOME INCInitial data: IM-1021 · B-cell lymphoma (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$IMNMIMMUNOME INCMarketing authorization application: varegacestat (formerly AL102). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IMTXIMMATICS NVInitial data: IMA402 · melanoma and gynecologic cancers (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IMTXIMMATICS NVClinical data readout: IMA203CD8 · Gynecologic cancers (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Later in 2026$IMUXImmunic, Inc.Planned initiation of the Phase 3 program of vidofludimus calcium in progressive multiple sclerosis, which the company expects to initiate later this year (stated October 21, 2026). Exact day not announced.Estimated windowPrimary source
By year-end 2026$IMUXImmunic, Inc.Top-line results from the fully enrolled Phase 3 ENSURE trials of vidofludimus calcium in relapsing multiple sclerosis, expected by year-end 2026 (stated October 21, 2026). Exact day not announced.Estimated windowPrimary source
H2 2026$IMVTIMMUNOVANT INCClinical program update: imeroprubart (IMVT-1402) · difficult-to-treat rheumatoid arthritis (RA) (potentially registrational). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H2 2026$IMVTIMMUNOVANT INCTopline data: imeroprubart (IMVT-1402) · Cutaneous lupus erythematosus; rheumatoid arthritis (RA). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q4 2026$INBXINHIBRX BIOSCIENCES INCFDA meeting: ozekibart (INBRX-109) · colorectal cancer (CRC) (Phase 1). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
2026$IOVAIOVANCE BIOTHERAPEUTICS INCConference presentation: Amtagvi (lifileucel) · metastatic non-squamous NSCLC. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
2026$IOVAIOVANCE BIOTHERAPEUTICS INCRegulatory decision: Amtagvi (lifileucel) · Advanced melanoma. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$IPHAInnate Pharma S.A.PACIFIC-9 Phase 3 monalizumab readout. Estimated window: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$IRDOpus Genetics, Inc.Planned initiation of a Phase 1/2 trial of OPGx-RDH12, AAV gene therapy for RDH12-associated Leber congenital amaurosis, after FDA clearance of the IND announced October 21, 2026; the company plans to initiate the trial this quarter (Q4 2026). Exact day not announced.Estimated windowPrimary source
Late 2026$IRONDISC MEDICINE INCInitial data: DISC-3405 · sickle cell disease (SCD) (Phase 1b). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
By end of 2026$IRONDisc Medicine, Inc.Planned resubmission of the New Drug Application for bitopertin in erythropoietic protoporphyria (EPP) to the U.S. FDA by the end of 2026, based on the positive APOLLO Phase 3 results; the company anticipates an FDA decision by mid-2027. Company plan; no date announced.Estimated windowPrimary source
SEC filing
Late 2026$IRONDISC MEDICINE INCFDA meeting: selcodebart (DISC-0974) · anemia of MF (Phase 2). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$IVAInventiva S.A.NATiV3 Phase 3 lanifibranor topline in MASH. Estimated: Q4 2026. Last patient visit completed; exact readout day unannounced.Estimated windowPrimary source
2026$JANXJANUX THERAPEUTICS INCFull data: JANX008 · Solid tumors (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$JANXJanux Therapeutics, Inc.JANX011 Phase 1 initial clinical data in healthy volunteers. Estimated window: H2 2026. Exact event day is not announced. Healthy-volunteer data are not efficacy data in autoimmune patients.Estimated windowPrimary source
Q4 2026$KODKodiak SciencesZenkuda multi-indication BLA submission planned. Estimated window: Q4 2026. Five positive Phase 3 studies across wet AMD, diabetic retinopathy and retinal vein occlusion. This is a planned submission, not an accepted filing, approval or PDUFA date.Estimated windowPrimary source
December 2026$KODKodiak SciencesKSI-101 PEAK Phase 3 Pivotal Analysis 1 topline in macular edema secondary to inflammation, first 300-patient cohort. Estimated window: December 2026. No exact release day; separate from registry primary completion and Pivotal Analysis 2.Estimated windowPrimary source
Supporting source
Late 2026$KRYSKRYSTAL BIOTECH INCInterim data: KB407 · cystic fibrosis (CF) (Phase 1). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H2 2026$KRYSKRYSTAL BIOTECH INCNDA/BLA submission: VYJUVEK (beremagene geperpavec) · Dystrophic Epidermolysis Bullosa. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$KRYSKRYSTAL BIOTECH INCTopline data: beremagene geperpavec-svdt (KB803) · corneal abrasions in DEB patients (registrational). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026$KRYSKRYSTAL BIOTECH INCTopline data: KB801 · Neurotrophic keratitis (registrational). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q4 2026$KRYSKRYSTAL BIOTECH INCFDA meeting: KB407 · cystic fibrosis (CF) (registrational). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026$KRYSKRYSTAL BIOTECH INCFDA meeting: KB111 · Hailey-Hailey disease (HHD). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$KRYSKRYSTAL BIOTECH INCInterim data: KB111 · Hailey-Hailey Disease. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026$KYMRKYMERA THERAPEUTICS INCTopline data: KT-621 · Atopic dermatitis (AtD) (Phase 2b). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$KYMRKYMERA THERAPEUTICS INCClinical data readout: KT-579 (Phase 1). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$KYTXKyverna Therapeutics, Inc.miv-cel rolling BLA submission completion in SPS. Estimated window: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$LEGNLEGEND BIOTECH CORPInitial data: dual CD20/CD19-targeted cell therapy. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$LGNDLIGAND PHARMACEUTICALS INCNDA/BLA submission: Qtorin 3.9% rapamycin anhydrous gel (Qtorin rapamycin) · microcystic lymphatic malformations (microcystic LMs). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$LGNDLIGAND PHARMACEUTICALS INCTopline data: ersodetug · Tumor hyperinsulinism (Phase 3). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$LPCNLipocine Inc.Partner Verity plans Canadian TLANDO launch by year-end 2026 following Health Canada approval. Company guidance; no exact event day.Estimated windowPrimary source
2026$LQDALIQUIDIA CORPPlanned completion of the ASCENT open-label study assessing 52 weeks of YUTREPIA treatment in pulmonary hypertension associated with interstitial lung disease. Completion is not an announced public data-release date. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$MAIAMAIA Biotechnology, Inc.THIO-104 Phase 3 in third-line NSCLC targets 100 patients enrolled and dosed by year-end 2026, versus 65 enrolled as disclosed October 7. This is an interim recruitment target, not full trial enrollment or results. Company guidance; no exact event day announced.Estimated windowPrimary source
Trial registry
Later in 2026$MANEVERADERMICS INCLonger-term data from Part B of Phase 2/3 Study '302' of VDPHL01 in male pattern hair loss, extending the safety findings in men through 12 months, anticipated later in 2026. Company timing; no date announced.Estimated windowPrimary source
SEC filing
Q4 2026$MBXMBX BIOSCIENCES INCFirst-cohort results from the 12-week multiple-ascending-dose portion of the Phase 1 MBX 4291 obesity trial. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$MBXMBX BIOSCIENCES INCConference presentation: MBX 6180. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
2026$MGTXMEIRAGTX HOLDINGS PLCIND submission: native human leptin (Ribo-Leptin) · Metabolic disease. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
2026$MGTXMEIRAGTX HOLDINGS PLCNDA/BLA submission: botaretigene sparoparvovec · X-linked retinitis pigmentosa. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$MIRMMirum Pharmaceuticals, Inc.Brelovitug AZURE-4, the second pivotal chronic hepatitis delta study, topline expected in Q4 2026. AZURE-1 results released on 28 September are a distinct study.Estimated windowPrimary source
By year-end 2026$MNKDMANNKIND CORPIND submission: Ralinepag DPI (MNKD-1501). Company timing: By year-end 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$NAMSNEWAMSTERDAM PHARMA CO NVTopline data: obicetrapib · type 2 diabetes (T2D) or metabolic syndrome (Phase 3). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$NBTXNANOBIOTIX SAFull data: NBTXR3 · NSCLC (Phase 2). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$NKTRNEKTAR THERAPEUTICSConference presentation: NKTR-0165 (preclinical). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
2026$NRIXNURIX THERAPEUTICS INCConference presentation: bexobrutideg · Relapsed or refractory B-cell malignancies (Phase 1a/1b). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2026$NRIXNURIX THERAPEUTICS INCIND submission: bexobrutideg · Autoimmune and inflammatory diseases (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026$NUVBNUVATION BIO INCPreclinical drug-drug-conjugate platform update as Nuvation explores new candidates. No clinical patient-data release is specified. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$NVCRNOVOCURE LTDRegulatory decision: TTFields therapy · brain metastases from non-small cell lung cancer (NSCLC). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Around year-end 2026$OCSOculis Holding AGPREDICT-1 registrational symptoms trial in genotype-selected TNFR1-mediated dry eye disease remains on track for topline around year-end. The October 8 Eyecelerator showcase is not this readout. Company guidance; exact event day is not announced.Estimated windowPrimary source
Supporting source
Q4 2026$OCULOcular Therapeutix, Inc.AXPAXLI wet AMD NDA submission with interim SOL-R safety analysis. Estimated window: Q4 2026. Guidance reaffirmed after completed pre-NDA meeting. Submission is neither FDA acceptance nor approval.Estimated windowPrimary source
Q4 2026$ONCYOncolytics Biotech Inc.GOBLET Cohort 4: final results of pelareorep with atezolizumab in second-line and later squamous cell anal carcinoma, expected in Q4 2026. Company guidance; no date announced.Estimated windowSEC filing
Late 2026$OPKOPKO HEALTH INCIND submission: long-acting PTH tablet · Hypoparathyroidism. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$ORICORIC PHARMACEUTICALS INCInitial data: enozertinib · 1L EGFR exon 20 insertion non-small cell lung cancer (NSCLC). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$ORICORIC PHARMACEUTICALS INCRinzimetostat program update. The source does not specify an interim clinical-data release. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ORKAOruka Therapeutics, Inc.ORKA-004: planned entry into clinical development of the extended-half-life anti-TL1A antibody in Q4 2026. Phase 2 combination studies are a separate future milestone. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ORKAOruka Therapeutics, Inc.EVERLAST-B ORKA-001 Week 16 data. Estimated window: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
December 2026$ORKAOruka Therapeutics, Inc.EVERLAST-A ORKA-001 Week 52 data. Estimated window: December 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$OSTXOS Therapies IncorporatedCompany targets completion of BLA and conditional marketing authorization application submissions in Q4 2026. Phase 3 development remains necessary; filing targets do not establish approval. Exact event day is not announced.Estimated windowPrimary source
Around mid-Q4 2026$OSTXOS Therapies IncorporatedOST-HER2 confirmatory Phase 3 initiation. Estimated window: around mid-Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$PBLSPARABILIS MEDICINES INCFDA meeting: zolucatetide · Desmoid tumors (Phase 3). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$PCRXPacira BioSciences, Inc.Viatris/Pacira acquisition closing expected by year-end 2026, subject to tender of a majority of shares, expiration of the applicable regulatory waiting period and other customary conditions. Company guidance; no exact event day announced.Estimated windowPrimary source
Late 2026$PCRXPACIRA BIOSCIENCES INCTopline data: ZILRETTA · Osteoarthritis pain of the shoulder (Phase 3). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$PCRXPACIRA BIOSCIENCES INCTopline data: enekinragene inzadenovec (PCRX-201) · Osteoarthritis of the knee (Phase 2). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
2026$PCRXPACIRA BIOSCIENCES INCNDA/BLA submission: EXPAREL. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$PCSAProcessa Pharmaceuticals, Inc.VT7208 phase 2 initiation in peanut allergy planned for H2 2026. Company guidance in the October 5 SEC disclosure; the disclosure date is not necessarily the first announcement of this plan. Exact event day is not announced.Estimated windowPrimary source
H2 2026$PCSAProcessa Pharmaceuticals, Inc.VT7208 phase 2 initiation in chronic spontaneous urticaria planned for H2 2026. Company guidance in the October 5 SEC disclosure; the disclosure date is not necessarily the first announcement of this plan. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$PGENPRECIGEN INCPRGN-2009 pipeline update in HPV-driven cancers; the quoted guidance does not specify a clinical-data release. Company timing: By year-end 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$PRAXPraxis Precision MedicinesRelutrigine EMERALD Phase 3 topline in broad developmental and epileptic encephalopathies. Estimated window: Q4 2026. Separate from the December 27 SCN2A/SCN8A PDUFA and registry completion dates.Estimated windowPrimary source
Q4 2026$PTCTPTC THERAPEUTICS INCRolling NDA/BLA submission: ST-920 · Fabry disease (BLA-stage). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$PTCTPTC THERAPEUTICS INCFDA meeting: votoplam · Huntington's disease (HD) (Phase 3). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$PVLAPALVELLA THERAPEUTICS INCPalvella anticipates starting a Phase 2 trial of QTORIN pitavastatin in disseminated superficial actinic porokeratosis (DSAP) in Q4 2026. Company guidance; the October 12 release does not confirm initiation.Estimated windowCompany release
Q4 2026$QNCXIRulya Therapeutics Inc. (formerly Quince Therapeutics)LAM-001 Phase 2 study in sarcoidosis-associated pulmonary hypertension planned to initiate Q4 2026. Company guidance, not a confirmed day. IRulya is the current company name; QNCX changes to IRLA on October 12, 2026.Estimated windowPrimary source
Q4 2026$RAPPRAPPORT THERAPEUTICS INCInitial data: RAP-219 · focal onset seizures, long-term open-label extension of the Phase 2a trial (safety). Company timing: Q4 2026. Exact event day is not announced.Estimated windowSEC filing
Q4 2026$RAREULTRAGENYX PHARMACEUTICAL INCClinical data readout: rivunatpagene miziparvovec · Wilson disease Cyprus2+ (pivotal). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
2026$REPLREPLIMUNE GROUP INCFull data: TUDRIQEV (vusolimogene oderparepvec-wtpg) · skin cancers, including cutaneous squamous cell carcinoma (CSCC), ARTACUS (Phase 1b/2). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$REPLREPLIMUNE GROUP INCInitial data: RP2 (sturlimgene erparepvec) · hepatocellular carcinoma (HCC). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$RGNXREGENXBIO Inc.ATMOSPHERE and ASCENT pivotal surabgene lomparvovec topline in wet AMD. Estimated window: Q4 2026. Distinct from registry primary-completion dates. Exact release day is not announced.Estimated windowPrimary source
H2 2026$RHHBYRoche Holding AGPhase 2 petrelintide plus enicepatide (CT-388) combination trial planned to start H2 2026. Distinct from the already initiated petrelintide monotherapy Phase 3 program. Exact event day is not announced.Estimated windowPrimary source
Late 2026$RLAYRELAY THERAPEUTICS INCZovegalisib: regulatory feedback to confirm the planned Phase 3 design in first-line endocrine-sensitive breast cancer, expected by year-end 2026. This is not a marketing-approval decision. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$RLAYRELAY THERAPEUTICS INCZovegalisib: clinical data and regulatory update for the vascular-anomalies program, expected by year-end 2026. Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$RXRXRECURSION PHARMACEUTICALS INCFDA meeting: REC-4881 · FAP. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$RXRXRECURSION PHARMACEUTICALS INCInterim data: REC-1245 (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Mid-December 2026$RZLTRezolute, Inc.Topline data from the open-label Phase 3 upLIFT study of ersodetug in tumor hyperinsulinism, expected mid-December 2026. The study is fully enrolled with 16 participants (announced October 14, 2026); 7 of the 8 participants in the first half met the primary endpoint responder criterion. Company guidance; no exact date announced.Estimated windowSEC filing
2026$SANASana Biotechnology, Inc.SC451 IND filing and Phase 1/2 trial start goal. Estimated window: 2026. Company goal, conditional on nonclinical, manufacturing and regulatory execution. This event does not set a date for SG293 data.Estimated windowPrimary source
Q4 2026$SCYXSCYNEXIS, Inc.SCY-770 Phase 2 proof-of-concept initiation. Estimated window: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Supporting source
H2 2026$SENSSenseonics Holdings, Inc.Expected U.S. launch of the next-generation Eversense 365 mobile app developed with Welldoc during the second half of 2026, with availability in European markets early the following year. Exact day not announced.Estimated windowPrimary source
Q4 2026$SENSSenseonics Holdings, Inc.Planned commercial launch of the integrated Eversense 365 and iLet Bionic Pancreas system (Beta Bionics) following completion of integration activities in the fourth quarter of 2026, subject to required testing, validation activities and applicable regulatory requirements. Exact day not announced.Estimated windowPrimary source
Q4 2026$SLSSELLAS LIFE SCIENCES GROUP INCTopline data: tambiciclib · AML (Phase 2). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q4 2026$SMMTSummit Therapeutics Inc.EA2251 (NCT07765433), registration-enabling open-label Phase II/III study sponsored and conducted by the ECOG-ACRIN Cancer Research Group: ivonescimab plus gemcitabine and cisplatin versus pembrolizumab or durvalumab plus gemcitabine and cisplatin in first-line advanced biliary tract cancer, primary endpoint overall survival. Activation of U.S. clinical trial sites is expected to begin in the fourth quarter of 2026. Exact day not announced.Estimated windowPrimary source
Late 2026$SNDXSYNDAX PHARMACEUTICALS INCIND submission: SNDX-4321 · non-small cell lung cancer (NSCLC). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$SNDXSYNDAX PHARMACEUTICALS INCFull data: Revuforj (revumenib) · NUP98r acute leukemia. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$SNDXSYNDAX PHARMACEUTICALS INCConference presentation: Revuforj (revumenib). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$SNDXSyndax Pharmaceuticals, Inc.Axatilimab plus ruxolitinib Phase 2 topline in newly diagnosed chronic GVHD. Estimated: Q4 2026. Distinct from the Phase 3 corticosteroid combination. Exact event day is not announced.Estimated windowPrimary source
Supporting source
H2 2026$SRPTSAREPTA THERAPEUTICS INCSRP-1001: further multiple-ascending-dose data from the ongoing Phase 1/2 trial in facioscapulohumeral muscular dystrophy (FSHD), expected in H2 2026. These are early clinical results, with no precise release day announced. Company timing: H2 2026.Estimated windowPrimary source
Supporting source
H2 2026$SRPTSAREPTA THERAPEUTICS INCSRP-1003: further multiple-ascending-dose data from the ongoing Phase 1/2 trial in myotonic dystrophy type 1 (DM1), expected in H2 2026. These are early clinical results, with no precise release day announced.Estimated windowPrimary source
Supporting source
Late 2026$SRRKSCHOLAR ROCK HOLDING CORPTopline data: SRK-439 (Phase 1). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$SRZNSurrozenFirst patient dosing in DUET Phase 1b/2a for diabetic macular edema expected Q4 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$STOKStoke Therapeutics, Inc.Dosing of the third OSPREY cohort is expected to complete by year-end 2026. Dosing of the first two cohorts is complete; this is not the future clinical readout. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$SYRESPYRE THERAPEUTICS INCTopline data: SPY072 · psoriatic arthritis (PsA) and axial spondyloarthritis (axSpA). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$TCRXTScan Therapeutics, Inc.ALLOHA Phase 1 Cohort C updated TSC-101 clinical data. Estimated window: Q4 2026. Data guidance maintained despite a pause in further Phase 3 ALLOHA-2 enrollment; this is not Phase 3 topline.Estimated windowPrimary source
H2 2026$TGTXTG THERAPEUTICS INCNDA/BLA submission: BRIUMVI (ublituximab-xiiy). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$TNGXTANGO THERAPEUTICS INCInitial data: TNG456 · glioblastoma (GBM). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$TNGXTANGO THERAPEUTICS INCVopimetostat monotherapy data in lung cancer. Separate from the pancreatic-cancer combination data scheduled for ESMO. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$TRDATRDAENTR-601-44: open-label follow-up from ELEVATE-44-201 Cohort 1 (6 mg/kg), assessing longer-term safety and functional measures in exon-44-skipping-amenable Duchenne muscular dystrophy, expected by year-end 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$TRDATRDAVX-670: partner Vertex expects multiple-ascending-dose results from GALILEO Phase 1/2 in myotonic dystrophy type 1 in H2 2026, covering safety, muscle-biopsy splicing and preliminary functional measures. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$TRVITREVI THERAPEUTICS INCLAKE Phase 2b refractory-chronic-cough study: sample-size re-estimation analysis after half the participants complete treatment. This is an operational interim analysis, not the final topline efficacy readout. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$TTRXTurn Therapeutics Inc.GX-03 atopic dermatitis FDA Type B meeting planned in Q4 2026; not an approval or PDUFA date. Company guidance; no exact event day announced.Estimated windowPrimary source
2026$TVTXTRAVERE THERAPEUTICS INCNDA/BLA submission: FILSPARI (sparsentan) · Japan. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$URGNUROGEN PHARMA LTDIND submission: UGN-501 · high-grade non-muscle invasive bladder cancer (NMIBC). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$VERAVera TherapeuticsTRUTAKNA full-approval sBLA submission planned Q4 2026.Estimated windowPrimary source
H2 2026$VIRVIR BIOTECHNOLOGY INCInterim data: VIR-5818 · Solid tumors (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$VIRVIR BIOTECHNOLOGY INCTopline data: elebsiran and tobevibart · Chronic hepatitis delta (HDV) (Phase 3). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H2 2026$VRDNVIRIDIAN THERAPEUTICS INCInitial data: VRDN-008 (phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$VRDNVIRIDIAN THERAPEUTICS INCIND submission: anti-TSHR candidate · Graves' disease and TED. Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
2026$VRDNVIRIDIAN THERAPEUTICS INCDevelopment program update: VRDN-006. Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$VSTMVerastem, Inc.Planned opening of the TARGET-D 301 Phase 3 trial of VS-7375 (oral KRAS G12D ON/OFF inhibitor) in first-line metastatic pancreatic cancer by year-end 2026, after FDA alignment on the three-arm design (PFS and ORR dual primary endpoints). Company plan; no date announced.Estimated windowSEC filing
By year-end 2026$VSTMVerastem, Inc.TARGET-D 101: mature data from the 900 mg VS-7375 plus anti-EGFR cohort in metastatic colorectal cancer and initial data from the 600 mg VS-7375 plus cetuximab cohort in metastatic pancreatic cancer, expected by year-end 2026. Company guidance; no date announced.Estimated windowSEC filing
H2 2026$XNCRXENCOR INCConference presentation: XmAb541 (CLDN6 x CD3) · Advanced gynecologic and germ cell tumors (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$XNCRXENCOR INCClinical program update: XmAb657 (CD19 x CD3) · Idiopathic inflammatory myopathies (Phase 1). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$XNCRXENCOR INCInterim data: XmAb942 (Xtend TL1A) · Ulcerative colitis (UC) (Phase 2b). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$XNCRXENCOR INCNDA/BLA submission: obexelimab · Immunoglobulin G4-related disease. Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$XRTXXORTX Therapeutics Inc.XRx-026 gout IND submission. Estimated window: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
By year-end 2026$ZBIOZENAS BIOPHARMA INCInitial data: ZB021 (Phase 1). Company timing: By year-end 2026. Exact event day is not announced.Estimated windowPrimary source
Q4 2026$ZBIOZENAS BIOPHARMA INCTopline data: obexelimab · systemic lupus erythematosus (SLE) (Phase 2). Company timing: Q4 2026. Exact event day is not announced.Estimated windowPrimary source
H2 2026$ZBIOZENAS BIOPHARMA INCMarketing authorization application: obexelimab · Immunoglobulin G4-Related Disease (IgG4-RD). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
Late 2026$ZLABZAI LAB LTDIND submission: ZL-1311 (Phase 1). Company timing: Late 2026. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
H2 2026$ZLABZAI LAB LTDInitial data: ZL-1503 (IL-13/IL-31R) · atopic dermatitis (AtD) (Phase 1/1b). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
By year-end 2026$ZURAZura Bio LimitedNEXUS-PMR: planned initiation by year-end 2026 of a Phase 2 study of tibulizumab in adults with polymyalgia rheumatica, the third indication selected for the program after FDA feedback. Company plan; no date announced.Estimated windowSEC filing
Q4 2026$ZURAZura Bio LimitedTibuSHIELD: topline data from the Phase 2 study of tibulizumab, a bispecific antibody against IL-17 and BAFF, in adults with hidradenitis suppurativa, expected in Q4 2026. Enrollment is complete with 247 participants randomized. Company guidance; no date announced.Estimated windowSEC filing
H2 2026$ZYMEZYMEWORKS INCConference presentation: pasritamig · Advanced prostate cancer (Phase 1b). Company timing: H2 2026. Exact event day is not announced.Estimated windowPrimary source
2026$ZYMEZYMEWORKS INCIND submission: ZW209 (Phase 1). Company timing: 2026. Exact event day is not announced.Estimated windowPrimary source
January 2027$SXTP60 Degrees Pharmaceuticals, Inc.Company plans to request a pre-sNDA meeting in January 2027; this is a request target, not a confirmed meeting or an accepted application. Exact event day is not announced.Estimated windowPrimary source
Trial registry
January 2027$SXTP60 Degrees Pharmaceuticals, Inc.Final primary and secondary endpoint data for the hospitalized-babesiosis study expected January 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
February 2027$ANABANAPTYSBIO INCPDUFA: Jemperli (dostarlimab) · Untreated stage II/III dMMR/MSI-H locally advanced rectal cancer, AZUR-1 (pivotal). Company timing: February 2027. Exact event day is not announced. FDA target action date; approval is not assured.Estimated windowPrimary source
ANAB stock hub
February 2027$GSKGSK / AnaptysBioJemperli rectal-cancer FDA action target communicated as February 2027 only; potential earlier review through National Priority Voucher. Exact day not disclosed. Estimated window: February 2027.Estimated windowPrimary source
Early 2027$ACIUAC Immune SAFDA discussions on the future development path and Part 2 design of VacSYn, the Phase 2 trial of ACI-7104 in early Parkinson's disease. Estimated window: early 2027. No meeting date has been announced. This event does not concern ACI-24.060 or ABATE.Estimated windowPrimary source
Supporting source
Q1 2027$AEMDAethlon Medical, Inc.NOR-101 Phase 1a start, proposed merger. Estimated window: Q1 2027. Exact event day is not announced. Aethlon/North merger is proposed and conditional; NRTX is only a proposed future ticker.Estimated windowPrimary source
Q4 2026 or Q1 2027$ANABAnaptysBio / GSKJemperli litigation judgment anticipated Q4 2026 or Q1 2027; exact day unknown.Estimated windowPrimary source
ANAB stock hub
Q1 2027$ATYRaTyr Pharma, Inc.EFZO-CONNECT efzofitimod Phase 2 topline in systemic sclerosis-related ILD. Estimated window: Q1 2027. Exact event day is not announced. The September 24 update addresses the sarcoidosis protocol and does not replace this SSc-ILD readout guidance.Estimated windowPrimary source
Supporting source
Q1 2027$BMEABiomea Fusion, Inc.COVALENT-211 Phase 2 icovamenib Week 26 primary-endpoint topline in type 2 diabetes. Estimated: Q1 2027. Enrollment completed; the company readout guidance is separate from the registry primary completion date.Estimated windowPrimary source
Q1 2027$CRVOCervoMed Inc.Topline clinical data from the neflamapimod Phase 2a nfvPPA trial are expected in Q1 2027, separate from the 2026 biomarker presentations.Estimated windowPrimary source
Q1 2027$DMACDiaMedica Therapeutics Inc.ReMEDy2 Phase 2/3 trial of DM199 in acute ischemic stroke: on October 22, 2026 the company announced that the 200th participant had been enrolled, reaching the prespecified threshold for the interim analysis. The independent DSMB will conduct the interim analysis after the first 200 participants complete 90-day follow-up, to assess sample size re-estimation or stopping for futility; if the trial continues, the final sample size will range between 300 and 728 participants. The company remains blinded and expects the interim analysis to be completed in the first quarter of 2027.Estimated windowFinviz (news)
Q1 2027$DYNDYNE THERAPEUTICS INCTopline data: zeleciment basivarsen (DYNE-101) · Myotonic dystrophy type 1 (DM1) (Phase 1/2). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q1 2027$EDITEditas Medicine, Inc.Initial Phase 1/2 Strive safety and tolerability data expected in Q1 2027; not the later Part 1 efficacy topline. Company guidance; exact event day is not announced.Estimated windowPrimary source
Q1 2027$FLNAFilana Therapeutics, Inc.simufilam TSC epilepsy Phase 2a screening. Estimated window: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q4 2026 / Q1 2027$GLUEMonte Rosa Therapeutics, Inc.GEMINI-1 Phase 2 initiation in gout expected Q4 2026 or Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$INBXINHIBRX BIOSCIENCES INCInterim data: ozekibart (INBRX-109) · colorectal cancer (CRC) (Phase 1). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$IPHAInnate Pharma S.A.TELLOMAK-3 lacutamab first patient. Estimated window: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$LABTLakewood-Amedex Biotherapeutics Inc.Nu-3 gel Phase 2a topline in mildly infected diabetic foot ulcers expected in Q1 2027. Separate from preclinical urinary and pulmonary infection findings announced October 7. Company guidance; no exact event day.Estimated windowPrimary source
Q1 2027$LGNDLIGAND PHARMACEUTICALS INCTopline data: volixibat · cholestatic pruritus due to primary biliary cholangitis (PBC), VANTAGE (Phase 2b). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$MIRAMIRA Pharmaceuticals, Inc.Ketamir-2 Phase 2a site initiation. Estimated window: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$MIRMMIRUM PHARMACEUTICALS INCTopline data: volixibat · Cholestatic pruritus due to primary biliary cholangitis (PBC), VANTAGE (Phase 2b). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$NAMSNEWAMSTERDAM PHARMA CO NVInterim data: obicetrapib (Phase 3). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$NKTRNEKTAR THERAPEUTICSTopline data: rezpegaldesleukin · Moderate-to-severe atopic dermatitis (AtD). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$OCGNOcugen, Inc.OCU400 Phase 3 liMeliGhT topline in retinitis pigmentosa. Estimated window: Q1 2027. Exact event day is not announced. The Bahamas provisional authorization is separate from FDA approval.Estimated windowPrimary source
Q1 2027$ORKAORUKA THERAPEUTICS INCORKA-002: Week 16 data from ORCA-SURGE, the Phase 2 trial in moderate-to-severe plaque psoriasis, expected in Q1 2027 after accelerated guidance. Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$PALIPalisade Bio, Inc.ASCENTRA-CD Phase 2 Crohn's first patient. Estimated window: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$PBLSPARABILIS MEDICINES INCClinical data readout: zolucatetide · FAP. Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$PHVSPHARVARIS NVCREAATE Phase 3 Part 1 topline results for deucrictibant XR prevention of attacks of acquired angioedema due to C1-inhibitor deficiency. This is not the CHAPTER-3 hereditary-angioedema trial. Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q1 2027$PPCBPropanc Biopharma, Inc.First-in-human Phase 1b PRP trial in advanced solid tumors planned for Q1 2027 in Australia, with up to 50 patients. Animal-model results do not establish human efficacy. Company guidance; no exact event day.Estimated windowPrimary source
Q1 2027$QNCXIRulya Therapeutics Inc. (formerly Quince Therapeutics)LAM-001 Phase 2 data in bronchiolitis obliterans syndrome after lung transplantation expected Q1 2027. Company guidance, not a confirmed day. IRulya is the current company name; QNCX changes to IRLA on October 12, 2026.Estimated windowPrimary source
Q1 2027$RAPPRAPPORT THERAPEUTICS INCFDA meeting: RAP-219 · acute bipolar mania. End-of-Phase 2 meeting with the FDA to discuss the Phase 2 data and registrational trial design. Company timing: Q1 2027. Exact event day is not announced.Estimated windowSEC filing
Q1 2027$REPLREPLIMUNE GROUP INCPlanned transition of the REVEAL registration-directed RP2 study from Phase 2 to Phase 3 in metastatic uveal melanoma. This does not specify a public interim-data release. Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$RNACCartesian Therapeutics, Inc.Descartes-08 AURORA Phase 3 generalized myasthenia gravis data expected Q1 2027 per company guidance. Distinct from the ClinicalTrials.gov primary-completion estimate.Estimated windowPrimary source
Q1 2027$SEPNSEPTERNA INCInitial data: SEP-479 · Hypoparathyroidism (Phase 1). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$SIONSionna Therapeutics, Inc.AscenSION CF Phase 2a proof-of-concept trial of SION-451 + SION-2222 in adults with CF homozygous for F508del expected to begin Q1 2027. The previously disclosed PreciSION CF post-hoc analyses are not a new positive trial readout; its key activity endpoint was not achieved. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$SRPTSAREPTA THERAPEUTICS INCELEVIDYS: 12-week data from the full ENDEAVOR Cohort 8, expected in Q1 2027. Full cohort enrollment is separately expected by year-end 2026. Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Year-end 2026 / Q1 2027$TGTXTG THERAPEUTICS INCTopline data: subcutaneous BRIUMVI (ublituximab) (Phase 3). Company timing: Year-end 2026 / Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$TLSATiziana Life Sciences LtdTiziana completed enrollment and initiated dosing in all patients of its Phase 2 randomized, placebo-controlled trial of intranasal foralumab in early/mild Alzheimer's disease, evaluating the drug as monotherapy and in combination with the anti-amyloid therapies lecanemab (Leqembi) or donanemab; on October 16, 2026, Tiziana announced that the last patient has begun dosing. Key endpoints include neuroinflammation measured by TSPO-PET imaging, cognitive function, and amyloid/tau fluid biomarkers. Topline data are expected in the first quarter of 2027 (company guidance; exact day not announced).Estimated windowSEC filing
Q1 2027$TRAXFIRST TRACKS BIOTHERAPEUTICS INCTopline data: ANB033 · Celiac disease (Phase 1b). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$TRDATRDAENTR-601-44: ELEVATE-44-201 Cohort 2 multiple-ascending-dose data (12 mg/kg), expected in Q1 2027. Distinct from Cohort 1 open-label follow-up. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$TTRXTurn Therapeutics Inc.GX-03 hidradenitis suppurativa Phase 2a first dosing planned in Q1 2027, subject to development and capital availability. Company guidance; no exact event day.Estimated windowPrimary source
Q1 2027$TTRXTurn Therapeutics Inc.GX-03 atopic dermatitis Phase 2 topline expected in Q1 2027. Company guidance; no exact event day announced.Estimated windowPrimary source
Q1 2027$TYRATYRA BIOSCIENCES INCInitial data: oral dabogratinib · Achondroplasia (Phase 2). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$VIRVIR BIOTECHNOLOGY INCTopline data: elebsiran and tobevibart · Chronic hepatitis delta (HDV) (Phase 3). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q1 2027$VRDNVIRIDIAN THERAPEUTICS INCNDA/BLA submission: elegrobart · thyroid eye disease (TED). Company timing: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
Q1 2027$VSTMVerastem, Inc.Initial data from VS-7375 in combination with gemcitabine/nab-paclitaxel in first-line metastatic pancreatic cancer, expected in Q1 2027. Company guidance; no date announced.Estimated windowSEC filing
Q1 2027$XENEXenon Pharmaceuticals Inc.X-NOVA2 azetukalner Phase 3 MDD topline. Estimated window: Q1 2027. Exact event day is not announced.Estimated windowPrimary source
April 2027$ETONETON PHARMACEUTICALS INCExpected U.S. launch of LIBERVANT (diazepam) buccal film by Eton in April 2027, subject to final FDA approval, after the competing orphan exclusivity expires on January 10, 2027. Company expectation; no launch day announced.Estimated windowPrimary source
Mid-2027$CCCCC4 Therapeutics, Inc.Cemsidomide plus elranatamab Phase 1b data from all evaluated cohorts expected mid-2027. Separate from Phase 1 dexamethasone data presented September 25, 2026.Estimated windowPrimary source
Early 2027$ABSIABSCI CORPTopline data: ABS-201 · Pattern hair loss (PHL). Company timing: Early 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$AZNAstraZeneca PLCefzimfotase alfa PDUFA action for hypophosphatasia. Estimated window: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$BHCBAUSCH HEALTH COMPANIES INCPotential regulatory decision (company forecast): lumify (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$BIIBEisai Inc.AMETHYST Phase 3 portion in cutaneous lupus erythematosus expected to read out H1 2027; remains blinded. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$BMEABiomea Fusion, Inc.COVALENT-212 Phase 2 icovamenib Week 26 primary-endpoint topline on background GLP-1 therapy. Estimated window: Q2 2027. Enrollment was still ongoing at the time of the source release; the date remains guidance.Estimated windowPrimary source
Early 2027$BMYBRISTOL MYERS SQUIBBBristol Myers Squibb expects topline results from fully enrolled ALOFT-PPF in progressive pulmonary fibrosis in early 2027. This is a separate trial from ALOFT-IPF; no exact release date is announced.Estimated windowPrimary source
H1 2027$CLYMClimb Bio, Inc.CLYM116 NAVIGATE-2 Phase 2 initial data in IgA nephropathy. Estimated window: H1 2027. Exact event day is not announced. The study evaluates Q8W/Q12W dosing.Estimated windowPrimary source
Late 2026 / early 2027$COAGHEMAB THERAPEUTICS HOLDINGS INCClinical data readout: sutacimig · Factor VII deficiency (Phase 2). Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2026 / early 2027$COAGHEMAB THERAPEUTICS HOLDINGS INCInterim data: HMB-002 · Von Willebrand disease (Phase 1/2). Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Early Q2 2027$COYACoya Therapeutics, Inc.ALSTARS Phase 2/3 ALS topline expected early Q2 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$DFTXDefinium TherapeuticsDT120 ODT — NDA submission planned in 1H 2027.Estimated windowPrimary source
H1 2027$DNLIDENALI THERAPEUTICS INCClinical data readout: DNL151 (LRRK2 inhibitor) · Parkinson's disease (PD) (Phase 2a). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$DNLIDENALI THERAPEUTICS INCInitial data: DNL628 · Alzheimer's disease (AD) (Phase 1b). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Early 2027$DRTSALPHA TAU MEDICAL LTDInitial data: Alpha DaRT · pancreatic cancer (PDAC), IMPACT. Company timing: Early 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Late 2026 / early 2027$DRTSALPHA TAU MEDICAL LTDTopline data: Alpha DaRT · cutaneous squamous cell carcinoma ReSTART. Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$ERASERASCA INCInterim data: ERAS-0015. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$ETONETON PHARMACEUTICALS INCRegulatory decision: KHINDIVI (hydrocortisone). Company timing: Q2 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$GLUEMonte Rosa Therapeutics, Inc.GALAXY-1 Phase 2 initiation in hidradenitis suppurativa expected H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$GLUEMonte Rosa Therapeutics, Inc.GFORCE-2 Phase 2b initiation in coronary artery disease expected H1 2027; design subject to regulatory feedback. Exact event day is not announced.Estimated windowPrimary source
H1 2027$GPCRSTRUCTURE THERAPEUTICS INCTopline data: ACCG-2671. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Supporting source
H1 2027$HCWBHCW Biologics Inc.HCW11-018b solid-tumor IND submission remains planned for H1 2027 following FDA Type B guidance; neither IND submission nor clinical trial start has been confirmed. Company guidance, not an FDA decision date. Exact event day is not announced.Estimated windowPrimary source
Early 2027$HRMYHARMONY BIOSCIENCES HOLDINGS INCTopline data: BP-205 · Sleep-deprived healthy volunteers (Phase 1b). Company timing: Early 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$HRMYHARMONY BIOSCIENCES HOLDINGS INCTopline data: EPX-100 (clemizole hydrochloride) · Rare epilepsies: Dravet syndrome (DS) and Lennox-Gastaut syndrome (LGS) (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Early 2027$HROWHARROW INCTopline data: TRIESENCE · ocular inflammation and pain following cataract surgery (Phase 3). Company timing: Early 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$HROWHARROW INCPlanned MELT-300 NDA submission following completion of the nonclinical and pharmacokinetic studies needed for the application. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2026 / early 2027$IDYAIDEAYA BIOSCIENCES INCInitial data: IDE034 (B7H3/PTK7 bispecific TOP1i ADC) (Phase 1). Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
Early 2027$IMCRIMMUNOCORE HOLDINGS PLCInterim data: IMC-M113V (Phase 1/2). Company timing: Early 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$IMTXIMMATICS NVTopline data: anzutresgene autoleucel (anzu-cel, IMA203) · Unresectable or metastatic melanoma (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$IOVAIOVANCE BIOTHERAPEUTICS INCRegulatory decision: Amtagvi (lifileucel) · melanoma. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$IOVAIOVANCE BIOTHERAPEUTICS INCInitial data: Amtagvi (lifileucel) · cutaneous squamous cell carcinoma (CSCC) and Merkel cell carcinoma (MCC). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
By mid-2027$IRONDISC MEDICINE INCRegulatory decision: bitopertin in erythropoietic protoporphyria (EPP). After the positive APOLLO Phase 3 results, Disc plans to resubmit the NDA to the FDA by the end of 2026, with an FDA decision anticipated by mid-2027. Company timing; no date announced.Estimated windowPrimary source
SEC filing
SEC filing
H1 2027$IVAInventiva S.A.Planned lanifibranor regulatory submission following NATiV3. Estimated window: H1 2027. Conditional on favorable NATiV3 results; filing is not approval.Estimated windowPrimary source
H1 2027$JANXJanux Therapeutics, Inc.JANX007 additional clinical data at a future medical congress. Estimated window: H1 2027. Congress and presentation day are not identified.Estimated windowPrimary source
H1 2027$KARDKARDIGAN INCTopline data: Tonlamarsen · Acute severe hypertension (Phase 2). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$KARDKARDIGAN INCTopline data: Danicamtiv · Genetic dilated cardiomyopathy (Phase 2b). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$KARDKARDIGAN INCTopline data: Ataciguat · Calcific aortic valve stenosis (Phase 2b). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$KODKodiak SciencesKSI-101 BLA submission planned. Estimated window: Q2 2027. Company forward-looking plan dependent on development and regulatory execution; no exact filing day, acceptance, approval or PDUFA date announced.Estimated windowPrimary source
Q2 2027$KODKodiak Sciences Inc.KSI-101 Pivotal Analysis 2 (PEAK plus PINNACLE) topline expected Q2 2027 in macular edema secondary to inflammation. Distinct from PEAK Pivotal Analysis 1 in December 2026 and the separate BLA submission plan. Exact event day is not announced.Estimated windowPrimary source
H1 2027$KRROKorro Bio, Inc.KRRO-111 (RNA-editing oligonucleotide for alpha-1 antitrypsin deficiency): regulatory submission expected in the first half of 2027, with the company planning to advance the program into the clinic in the same period. Current data are preclinical. Exact day not announced.Estimated windowPrimary source
H1 2027$KRROKorro Bio, Inc.KRRO-121 dosing in patients with urea-cycle disorders is expected to start in H1 2027, subject to regulatory approval. This is separate from the healthy-volunteer component. Exact event day is not announced.Estimated windowPrimary source
H1 2027$KRYSKRYSTAL BIOTECH INCInterim data: KB707 · Solid tumors of the lung (Phase 1/2). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$LBRXLB PHARMACEUTICALS INCTopline data: LB-102 · schizophrenia (SCZ), NOVA-2 (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$LGNDLIGAND PHARMACEUTICALS INCTopline data: avim therapy. Company timing: Q2 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$MANEVERADERMICS INCTopline data: VDPHL01 · Female pattern hair loss (Phase 2/3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2026 / early 2027$MAZEMAZE THERAPEUTICS INCInterim data: MZE829 · APOL1-mediated kidney disease (AMKD), broad patient population (Phase 2). Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$MGTXMEIRAGTX HOLDINGS PLCClinical data readout: AAV2-hAQP1 · Radiation-induced xerostomia (pivotal Phase 2). Company timing: Q2 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$MIRMMirum Pharmaceuticals, Inc.Company expects to submit a brelovitug BLA for chronic hepatitis delta to FDA in H1 2027. This is a half-year window.Estimated windowPrimary source
H1 2027$MIRMMirum Pharmaceuticals, Inc.Mirum plans a U.S. sNDA in H1 2027 based on positive EXPAND results in ultra-rare cholestatic liver diseases. Submission guidance; no FDA decision date is announced.Estimated windowPrimary source
Company release
H1 2027$MIRMMIRUM PHARMACEUTICALS INCNDA/BLA submission: volixibat · cholestatic pruritus due to primary sclerosing cholangitis (PSC). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$MLTXMoonLake ImmunotherapeuticsIZAR-1 sonelokimab Phase 3 full Week 52 readout in psoriatic arthritis. Estimated: H1 2027. The trial remains blinded through Week 52. Exact event day is not announced.Estimated windowPrimary source
Early 2027$NKTRNektar TherapeuticsZENITH AA, single registrational Phase 3 study of rezpegaldesleukin in severe-to-very-severe alopecia areata (850 patients; primary endpoint SALT Score ≤20 at Week 52), expected to initiate in early 2027. ESTIMATED window: early 2027. Exact day not announced.Estimated windowSEC filing
SEC filing
Supporting source
H1 2027$NVONovo NordiskDenecimig US launch targeted H1 2027 conditional on approval; no FDA action date has been communicated after the manufacturing-related review extension. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$OCGNOcugen, Inc.OCU400 planned BLA submission for retinitis pigmentosa. Estimated window: Q2 2027. Exact event day is not announced; a planned filing is not FDA acceptance or approval.Estimated windowPrimary source
H1 2027$ONCYOncolytics Biotech Inc.GOBLET Cohort 5: initial results of pelareorep-based therapy with chemotherapy, with and without atezolizumab, in first-line metastatic pancreatic ductal adenocarcinoma, expected in the first half of 2027; the company said timing could be extended as multiple patients continue treatment and follow-up. Company guidance; no date announced.Estimated windowSEC filing
H1 2027$OPKOPKO HEALTH INCInitial data: MDX2004 (Phase 1). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2026 / early 2027$OPKOPKO HEALTH INCInitial data: MDX2301 · prevention of COVID-19 (Phase 1). Company timing: Late 2026 / early 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$PBLSPARABILIS MEDICINES INCClinical data readout: zolucatetide · ACP. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$PCSAProcessa Pharmaceuticals, Inc.VT7208 phase 2 initiation in relapsing multiple sclerosis planned for H1 2027. Company guidance in the October 5 SEC disclosure; the disclosure date is not necessarily the first announcement of this plan. Exact event day is not announced.Estimated windowPrimary source
H1 2027$PCVXVAXCYTE INCClinical data readout: VAX-31 · invasive pneumococcal disease and pneumonia, OPUS-2 and OPUS-3 (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$PHARPharming Group N.V.Napazimone (KL1333) for mtDNA-driven mitochondrial disease: enrollment of the pivotal FALCON trial now expected to be completed in the first half of 2027, with approximately 145 of the planned 180 subjects enrolled by the end of 2026. Topline results are expected approximately one year after enrollment completion. Exact day not announced.Estimated windowPrimary source
H1 2027$PHVSPHARVARIS NVNDA/BLA submission: deucrictibant XR (PHVS719) · HAE CHAPTER-3 (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$PVLAPALVELLA THERAPEUTICS INCRegulatory decision: sirolimus (QTORIN rapamycin) · Microcystic lymphatic malformations (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$QUREUNIQURE NVConference presentation: AMT-260 · Refractory mesial temporal lobe epilepsy (Phase I/IIa). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RAPPRAPPORT THERAPEUTICS INCPhase 3 initiation: RAP-219 · primary generalized tonic-clonic seizures (PGTCS). Company timing: H1 2027. Exact event day is not announced.Estimated windowSEC filing
H1 2027$RAREULTRAGENYX PHARMACEUTICAL INCTopline data: avalotcagene ontaparvovec · ornithine transcarbamylase deficiency, Enh3ance (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RCUSARCUS BIOSCIENCES INCClinical data readout: quemliclustat · Metastatic pancreatic ductal adenocarcinoma (PDAC) (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RLAYRELAY THERAPEUTICS INCZovegalisib plus atirmociclib and endocrine therapy: Phase 1/2 triplet clinical-data update in breast cancer, expected in H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RNXTRenovoRxTIGeR-PaC Phase 3 in locally advanced pancreatic cancer: trial completion expected in H1 2027; enrollment completed in August 2026. Separate from the H2 2027 public topline. Company guidance; no exact event day announced.Estimated windowPrimary source
H1 2027$RXRXRECURSION PHARMACEUTICALS INCInterim data: REC-3565 (Phase 1). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RXRXRECURSION PHARMACEUTICALS INCInterim data: REC-617 (Phase 1). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$RXRXRECURSION PHARMACEUTICALS INCInitial data: REC-4881 · familial adenomatous polyposis (FAP) (Phase 1b/2). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$SCTXScribe Therapeutics Inc.STX-1150 Phase 1 initial single-ascending-dose clinical data. Estimated window: H1 2027. Planned data include safety, tolerability and LDL-C lowering. Exact event day is not announced.Estimated windowPrimary source
H1 2027$SRRKScholar Rock Holding CorporationScholar Rock expects a CHMP opinion on the resubmitted SMA application in H1 2027. Company guidance, not a confirmed regulator action date or European Commission approval. Exact event day is not announced.Estimated windowPrimary source
H1 2027$STOKSTOKE THERAPEUTICS INCInitial safety and efficacy data from OSPREY cohorts 3 and 4 are expected in H1 2027. First two dose cohorts are complete; fourth-cohort dosing is subject to ongoing safety assessments. Exact event day is not announced.Estimated windowPrimary source
H1 2027$STOKSTOKE THERAPEUTICS INCCompany plans to submit data throughout H1 2027 in support of the zorevunersen NDA for Dravet syndrome. Submission completion is separately guided for H2 2027 after the Q3 EMPEROR readout. Exact event day is not announced.Estimated windowPrimary source
H1 2027$TARSTARSUS PHARMACEUTICALS INCTP-04 lotilaner ophthalmic-gel Phase 2 KORE topline results in ocular rosacea. TP-05/Calliope is a separate oral Lyme-disease prevention program. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$TCRXTScan Therapeutics, Inc.TSC-101 update on patients treated with the commercial-ready manufacturing process. Estimated: Q2 2027. Company continues patient follow-up despite enrollment pause; exact day not announced.Estimated windowPrimary source
H1 2027$TLXTelix Pharmaceuticals LimitedOPTIMAL-PSMA, Phase 2 study of TLX597-Tx (177Lu-DOTA-HYNIC-panPSMA) in metastatic androgen pathway modulator-resistant prostate cancer: enrollment of 120 patients completed; data readout expected in the first half of 2027. Exact day not announced.Estimated windowFinviz (news)
H1 2027$TLXTELIX PHARMACEUTICALS LTDCOMPOSE Phase 3 second interim analysis of ITM-11 in G2/G3 somatostatin-receptor-positive gastroenteropancreatic neuroendocrine tumors. Telix announced an agreement to acquire ITM; as of September 21, 2026, closing remained subject to conditions. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H1 2027$TRAXFIRST TRACKS BIOTHERAPEUTICS INCPhase 2 development of ANB033 in vitiligo and one additional indication is planned for H1 2027; the additional indication and exact start date are not disclosed.Estimated windowCompany release
H1 2027$TRDATRDAENTR-601-45: ELEVATE-45-201 Cohort 2 multiple-ascending-dose data at 10 mg/kg, expected in H1 2027. Distinct from ELEVATE-44-201 Cohort 2. Exact event day is not announced.Estimated windowPrimary source
H1 2027$TSHATAYSHA GENE THERAPIES INCTopline data: TSHA-102 · Rett syndrome (RTT), REVEAL (pivotal). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$VORVOR BIOPHARMA INCTopline data: telitacicept · Generalized myasthenia gravis (gMG) (Phase 3). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
Q2 2027$VSTMVerastem, Inc.Initial data from the Phase 2 TARGET-D 201 trial of VS-7375 in second-line pancreatic cancer, expected in Q2 2027 (enrollment expected to complete by year-end 2026). Company guidance; no date announced.Estimated windowSEC filing
H1 2027$XNCRXENCOR INCInitial data: XmAb412 · Autoimmune and inflammatory disease. Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
H1 2027$ZLABZAI LAB LTDInitial data: ZL-1503 (IL-13/IL-31R) · atopic dermatitis (AtD) (Phase 1/1b). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
H1 2027$ZLABZAI LAB LTDTopline data: ZL-6201 · sarcoma and selected tumors (Phase 1a/b). Company timing: H1 2027. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
H1 2027$ZNTLZentalis Pharmaceuticals, Inc.DENALI Part 2 integrated azenosertib topline in Cyclin E1-positive platinum-resistant ovarian cancer. Estimated window: H1 2027. Exact event day is not announced. Potential accelerated-approval support is conditional, not approval.Estimated windowPrimary source
Supporting source
H1 2027$ZURAZura Bio LimitedTibuSURE: topline data from the Phase 2 study of tibulizumab in adults with systemic sclerosis, expected in the first half of 2027. Enrollment is complete with 91 participants randomized. Company guidance; no date announced.Estimated windowSEC filing
Mid-2027$AEMDAethlon Medical, Inc.NOR-101 Phase 1a interim PK and safety data, proposed merger. Estimated window: mid-2027. Exact event day is not announced. Aethlon/North merger is proposed and conditional; NRTX is only a proposed future ticker.Estimated windowPrimary source
Mid-2027$COAGHemab Therapeutics Holdings, Inc.HMB-003 initial clinical data. Estimated window: mid-2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027$JAGXJaguar Health, Inc.crofelemer MVID NDA filing. Estimated window: mid-2027. Exact event day is not announced. Subject to study completion and regulatory alignment.Estimated windowPrimary source
Mid-2027$KYTXKyverna Therapeutics, Inc.KYSA-6 Phase 3 miv-cel enrollment completion. Estimated window: mid-2027. Exact event day is not announced.Estimated windowPrimary source
By July 2027; exact day unspecified$RHHBYF. Hoffmann-La Roche LtdRoche expects an FDA approval decision for vamikibart in uveitic macular edema by July 2027. BLA acceptance is confirmed; the company release did not disclose an exact FDA action date.Estimated windowPrimary source
Q3 2027$ACADACADIA PHARMACEUTICALS INCTopline data: ACP-211 · major depressive disorder (MDD) (Phase 2). Company timing: Q3 2027. Exact event day is not announced.Estimated windowPrimary source
Q3 2027$BCRXBIOCRYST PHARMACEUTICALS INCTopline data: navenibart · hereditary angioedema (HAE) (pivotal). Company timing: Q3 2027. Exact event day is not announced.Estimated windowPrimary source
Q3 2027$DYNDYNE THERAPEUTICS INCNDA/BLA submission: zeleciment basivarsen (DYNE-101) · myotonic dystrophy type 1 (DM1) (Phase 1/2). Company timing: Q3 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Q3 2027$RAPPRAPPORT THERAPEUTICS INCPhase 1 data: RAP-219 long-acting injectable formulation · pharmacokinetic data. Company timing: Q3 2027. Exact event day is not announced.Estimated windowSEC filing
Q3 2027$STOKSTOKE THERAPEUTICS INCClinical data readout: zorevunersen · Dravet syndrome (DS) (Phase 3). Company timing: Q3 2027. Exact event day is not announced.Estimated windowPrimary source
Q3 2027$TRAXFIRST TRACKS BIOTHERAPEUTICS INCTopline data: ANB033 · eosinophilic esophagitis (EoE) (Phase 1b). Company timing: Q3 2027. Exact event day is not announced.Estimated windowPrimary source
Q3 2027$TTRXTurn Therapeutics Inc.GX-03 hidradenitis suppurativa Phase 2a topline expected in Q3 2027, conditional on execution and funding. Company guidance; no exact event day.Estimated windowPrimary source
Mid-2027$VTVTvTv Therapeutics Inc.CATT1 Phase 3 topline in type 1 diabetes expected mid-2027. Distinct from registry primary completion. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$ABCLABCELLERA BIOLOGICS INCIND submission: ABCL688 · Autoimmunity. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$ABSIABSCI CORPInterim data: ABS-201 · Endometriosis, HEADLINE (Phase 2). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$ABVXABIVAX SATopline data: obefazimod · Crohn's disease (CD) (Phase 2b). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$ALKSALKERMES PLCClinical data readout: ALKS 7290 · attention-deficit hyperactivity disorder (ADHD) (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$ALMRALAMAR BIOSCIENCES INCDevice marketing authorization submission: ARGO HT/DX instrument. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$ALTAltimmune, Inc.RESTORE Phase 2 pemvidutide topline in alcohol-associated liver disease. Estimated window: H2 2027. Enrollment completed in July 2026. The topline concerns the updated 48-week endpoint, not enrollment. Exact release day is not announced.Estimated windowPrimary source
2027$AMLXAMYLYX PHARMACEUTICALS INCIND submission: AMX0318 · PBH and other rare diseases. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$ARWRArrowhead PharmaceuticalsData from the early Alzheimer's disease cohorts of the ARO-MAPT Phase 1/2a study, expected in 2027 per Arrowhead's October 14, 2026 release. The October 14 interim healthy-volunteer data showed mean CSF tau reductions of 40%, 69% and 73% at Day 105 (maximum 85%). Company expectation; no date announced.Estimated windowPrimary source
H2 2027$AVLNAVALYN PHARMA INCTopline data: ap01 (inhaled pirfenidone) · Progressive pulmonary fibrosis (Phase 2b). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2027$AVLNAVALYN PHARMA INCTopline data: ap02 (inhaled nintedanib) · idiopathic pulmonary fibrosis (IPF) (Phase 2). Company timing: Late 2027. Exact event day is not announced.Estimated windowPrimary source
2027$AXSMAXSOME THERAPEUTICS INCTopline data: solriamfetol · shift work disorder, SUSTAIN (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$BCAXBICARA THERAPEUTICS INCInterim data: ficerafusp alfa · 1L R/M HPV-negative HNSCC, FORTIFI-HN01 (Phase 3). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
Late 2027$BCRXBIOCRYST PHARMACEUTICALS INCNDA/BLA submission: navenibart. Company timing: Late 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$BIOABioAge Labs, Inc.QUELL-DME BGE-102 Phase 2 topline in diabetic macular edema. Estimated window: H2 2027. Exact event day is not announced. Primary endpoint is BCVA change at week 12.Estimated windowPrimary source
H2 2027$BRVEBRAVEHEART BIO INCInterim data: BHB-1893 · obstructive HCM ("oHCM") (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
2027$CLDXCelldex Therapeutics, Inc.barzolvolimab CSU BLA submission. Estimated window: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$CNMDCONMED CORPClinical data readout: BioBrace · rotator cuff. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$DFTXDEFINIUM THERAPEUTICS INCTopline data: DT120 ODT · Major depressive disorder (MDD) (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$DMRADAMORA THERAPEUTICS INCInitial data: DMR-001 · essential thrombocythemia (ET) and myelofibrosis (MF). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$DMRADAMORA THERAPEUTICS INCIND submission: DMR-003. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$DNLIDENALI THERAPEUTICS INCInitial data: DNL952 · Pompe disease (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$DNLIDENALI THERAPEUTICS INCClinical data readout: DNL921 · Alzheimer's disease (AD) (Phase 1/1b). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$DNLIDENALI THERAPEUTICS INCClinical data readout: DNL593 · granulin (GRN)-related frontotemporal dementia (FTD-GRN) (Phase 1/2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$DNLIDENALI THERAPEUTICS INCNDA/BLA submission: zafinofusp alfa (DNL126; ETV:SGSH) · Sanfilippo syndrome type A (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
By year-end 2027$DNTHDIANTHUS THERAPEUTICS INCDNTH312 development target is Phase 1 readiness by year-end 2027. The quoted statement does not establish an IND filing date or first-patient dosing date. Company timing: By year-end 2027. Exact event day is not announced.Estimated windowPrimary source
Later in 2027; quarter unspecified$EDITEditas Medicine, Inc.Editas plans Part 1 dose-finding enrollment completion and topline safety/efficacy results later in 2027. The release does not specify a quarter. Company guidance; no exact event day announced.Estimated windowPrimary source
H2 2027$ETONETON PHARMACEUTICALS INCNDA/BLA submission: ASN-001 · Moderate infantile hemangiomas. Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$GLUEMonte Rosa Therapeutics, Inc.Initial GEMINI-1 Phase 2 gout data expected H2 2027. Exact event day is not announced.Estimated windowPrimary source
Q4 2027$HCMHUTCHMED (CHINA) LTDTopline data: IMG-007 · moderate-to-severe atopic dermatitis (AtD) (Phase 2b). Company timing: Q4 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$HRMYHARMONY BIOSCIENCES HOLDINGS INCTopline data: Pitolisant HD · Narcolepsy; idiopathic hypersomnia (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$HRMYHARMONY BIOSCIENCES HOLDINGS INCPitolisant (WAKIX): topline data from the Phase 3 TEMPO study in Prader-Willi syndrome are expected around mid-2027. This is distinct from pitolisant GR in narcolepsy. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$IDYAIDEAYA BIOSCIENCES INCInterim data: darovasertib combination · Metastatic uveal melanoma. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$IMCRIMMUNOCORE HOLDINGS PLCInitial data: IMC-R117C · advanced solid tumors, including colorectal cancer (CRC) (Phase 1/2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$IMTXIMMATICS NVIMA401 (MAGEA4/8) plus IMA402 (PRAME): first clinical data from the combination cohort in squamous non-small-cell lung cancer expected in 2027. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$IMTXIMMATICS NVAnzu-cel BLA submission planned in 2027 after final SUPRAME progression-free-survival topline data expected in the first half of 2027. The newer August guidance no longer specifies a first-half filing deadline. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$IMVTIMMUNOVANT INCTopline data: imeroprubart (IMVT-1402) · Graves' disease (potentially registrational). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$IMVTIMMUNOVANT INCTopline data: imeroprubart (IMVT-1402) · myasthenia gravis (gMG) (potentially registrational). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Mid-2027 (approximate)$INBXINHIBRX BIOSCIENCES INCInitial data: INBRX-106 · non-small cell lung cancer (NSCLC) (Phase 1/2). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
H2 2027$IONSIONIS PHARMACEUTICALS INCClinical data readout: obudanersen · Angelman syndrome, REVEAL (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
IONS stock hub
2027$IONSIONIS PHARMACEUTICALS INCNDA/BLA submission: ZANVASTRO (zilganersen). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
IONS stock hub
2027$IOVAIOVANCE BIOTHERAPEUTICS INCMarketing authorization resubmission: Amtagvi (lifileucel) · Advanced melanoma. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$IRONDISC MEDICINE INCInitial data: selcodebart (DISC-0974) · inflammatory bowel disease (IBD) (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
By Q4 2027$KAPAKairos PharmaCompany expects trial completion in or before Q4 2027, following protocol modification and randomized enzalutamide with or without ENV105. This is completion guidance, not a confirmed results date. Exact event day is not announced.Estimated windowPrimary source
2027$KLRAKAILERA THERAPEUTICS INCClinical data readout: HRS-7535 (KAI-7535) · Obesity (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$KLRAKAILERA THERAPEUTICS INCClinical data readout: HRS-4729 (KAI-4729) (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$KLRAKAILERA THERAPEUTICS INCRibupatide injection: Phase 2b high-dose obesity data in 264 participants with BMI at least 35 and no type 2 diabetes. The 48-week trial evaluates 10, 13, 16 and 20 mg weekly doses; data anticipated around mid-2027. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
Supporting source
H2 2027$KRROKorro Bio, Inc.Interim clinical readout from the KRRO-121 ANCHOR program expected in H2 2027 according to company guidance. Exact event day is not announced.Estimated windowPrimary source
2027$KRYSKRYSTAL BIOTECH INCInterim data: KB408 · alpha-1 antitrypsin deficiency (AATD) lung disease (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2027$KYMRKYMERA THERAPEUTICS INCIND submission: KT-200 · breast cancer and other solid tumors. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2027$KYMRKYMERA THERAPEUTICS INCClinical data readout: KT-621 · Asthma (Phase 2b). Company timing: Late 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LBRXLB PHARMACEUTICALS INCFDA meeting: LB-102 · schizophrenia (SCZ) (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LGNDLIGAND PHARMACEUTICALS INCTopline data: lasofoxifene · metastatic breast cancer, ELAINE-3 (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LGNDLIGAND PHARMACEUTICALS INCTopline data: Qtorin 3.9% rapamycin anhydrous gel (Qtorin rapamycin) · Angiokeratomas (Phase 2). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LPCNLipocine Inc.Topline data: LPCN 1154 (oral brexanolone) · severe postpartum depression, BLOOM Phase 3 (randomized, double-blind, placebo-controlled US study, N=120; primary endpoint HAM-D17 change from baseline at Hour 60 versus placebo). Company timing: 2H 2027. Exact event day is not announced.Estimated windowSEC filing
Q4 2027$LSTALisata Therapeutics, Inc.MAR002 acromegaly Phase 2 topline. Estimated window: Q4 2027. Exact event day is not announced.Estimated windowPrimary source
Q4 2027$LSTALisata Therapeutics, Inc.MAR001 severe hypertriglyceridemia Phase 2b topline. Estimated window: Q4 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LTGOLatigo Biotherapeutics, Inc.LTG-321 Phase 2 topline in osteoarthritis knee pain. Estimated window: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LTGOLatigo Biotherapeutics, Inc.Onzotrigine Phase 3 bunionectomy and open-label safety topline. Estimated window: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$LXEOLexeo Therapeutics, Inc.SUNRISE-FA 2 LX2006 topline. Estimated window: H2 2027. Exact event day is not announced.Estimated windowPrimary source
2027$MAIAMAIA Biotechnology, Inc.THIO-104 Phase 3 interim analysis in third-line NSCLC targeted in 2027. The issuer does not specify a quarter or public release day. Company guidance; no exact event day.Estimated windowPrimary source
Trial registry
2027$MAZEMAZE THERAPEUTICS INCTopline data: MZE782 · phenylketonuria (PKU) (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$MBXMBX BIOSCIENCES INCMBX 4291: topline results from the Phase 1 obesity study are anticipated in 2027. The program studies single and multiple ascending doses of a GLP-1/GIP co-agonist prodrug; this overall readout is distinct from the first 12-week cohort update in Q4 2026. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
Mid-2027 (approximate)$MESOMESOBLAST LTDTopline data: rexlemestrocel-l · chronic low back pain (CLBP) (Phase 3). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$MESOMESOBLAST LTDNDA/BLA submission: rexlemestrocel-l · Chronic low back pain (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$MGTXMEIRAGTX HOLDINGS PLCNDA/BLA submission: AAV2-hAQP1 · Radiation-induced xerostomia (pivotal). Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$MIRMMIRUM PHARMACEUTICALS INCTopline data: MRM-3379 · Fragile X syndrome, BLOOM (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$MIRMMIRUM PHARMACEUTICALS INCTopline data: brelovitug · chronic hepatitis delta virus (HDV) infection, AZURE-2 and AZURE-3 (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$MIRMMIRUM PHARMACEUTICALS INCPotential US regulatory approval of brelovitug after the planned H1 2027 BLA submission, subject to FDA review. The September 28 update targets a potential US commercial launch in Q4 2027 if approved. Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
Late 2027$MNKDMANNKIND CORPClinical data readout: insulin human (Afrezza) · newly diagnosed type 1 diabetes (T1D). Company timing: Late 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$NGENNervGenRESTORE Phase 3 enrollment completion is expected in H2 2027. The study plans approximately 150 participants; this is a recruitment milestone, not a results date.Estimated windowCompany release
Trial registry
2027$NKTRNEKTAR THERAPEUTICSInitial data: rezpegaldesleukin · type 1 diabetes mellitus (T1D) (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$NUVBNUVATION BIO INCClinical data readout: safusidenib · grade 3 IDH1-mutant oligodendroglioma. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$OGNORGANON & CORegulatory decision: Nexplanon. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$PCSAProcessa Pharmaceuticals, Inc.VT7208 proof-of-concept data in peanut allergy planned for H2 2027. Company guidance in the October 5 SEC disclosure; the disclosure date is not necessarily the first announcement of this plan. Exact event day is not announced.Estimated windowPrimary source
H2 2027$PCVXVAXCYTE INCTopline data: VAX-A1 · Disease caused by Group A Streptococcus (Phase 1). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PODDINSULET CORP510(k) submission: fully closed-loop automated insulin delivery (AID) system · Type 2 diabetes (T2D), EVOLVE (pivotal). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PRAXPRAXIS PRECISION MEDICINES INCTopline data: elsunersen · SCN2A DEE (EMBRAVE3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PRAXPRAXIS PRECISION MEDICINES INCNDA/BLA submission: vormatrigine · focal onset seizures (FOS), POWER1 and POWER2 (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PRAXPRAXIS PRECISION MEDICINES INCNDA/BLA submission: relutrigine · SCN2A and SCN8A DEEs, EMERALD. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PRAXPRAXIS PRECISION MEDICINES INCTopline data: vormatrigine · FOS (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$PRMEPrime MedicineInitial PM577a Phase 1/2 clinical data in H1069Q-mutated Wilson disease expected during 2027. Exact event day is not announced.Estimated windowPrimary source
Trial registry
H2 2027$PVLAPALVELLA THERAPEUTICS INCTopline data: sirolimus (QTORIN rapamycin) · Clinically significant angiokeratomas, LOTU (Phase 2). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$RAPPRAPPORT THERAPEUTICS INCPhase 1 data: RAP-641 · preliminary results. Company timing: H2 2027. Exact event day is not announced.Estimated windowSEC filing
H2 2027$RAPPRAPPORT THERAPEUTICS INCPhase 3 initiation: RAP-219 · acute bipolar mania. Start of two Phase 3 pivotal trials. Company timing: H2 2027. Exact event day is not announced.Estimated windowSEC filing
2027$RAPPRAPPORT THERAPEUTICS INCInitial data: RAP-219. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027; exact range unspecified$RCKTRocket Pharmaceuticals, Inc.Rocket guides pivotal Danon Phase 2 dosing completion to mid-2027. No exact day or quarter is given. Company guidance.Estimated windowPrimary source
Mid-2027 (approximate)$RCUSARCUS BIOSCIENCES INCAB102 proof-of-concept study milestone in chronic spontaneous urticaria. The quoted source forecasts the study, not a dated release of initial results. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$REGNRegeneron PharmaceuticalsThe three preclinical antibodies added to the Sanofi alliance, targeting IL-4xIL-13, IL-4 and IL-4Ralpha, are expected to enter clinical studies in 2027. Portfolio-level company guidance; specific study dates and indications not announced. Distinct from REGN20423, already in Phase 1. Exact event day is not announced.Estimated windowPrimary source
Supporting source
H2 2027$REPLREPLIMUNE GROUP INCRP1 (vusolimogene oderparepvec) plus nivolumab: interim overall-survival analysis from the randomized Phase 3 IGNYTE-3 trial in advanced melanoma is planned for H2 2027. This is distinct from the primary overall-survival readout expected in 2030. Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$RNXTRenovoRxTIGeR-PaC Phase 3 public topline in locally advanced pancreatic cancer expected in H2 2027. Company guidance; no exact event day.Estimated windowPrimary source
H2 2027$RXRXRECURSION PHARMACEUTICALS INCInterim data: REC-4539 (Phase 1). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$SABSSAB Biotherapeutics, Inc.SAFEGUARD SAB-142 Phase 2b topline. Estimated window: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$SCYXSCYNEXIS, Inc.SCY-770 Phase 2 early efficacy data. Estimated window: H2 2027. Exact event day is not announced.Estimated windowPrimary source
Supporting source
2027$SCYXSCYNEXIS, Inc.SCY-247: the company expects to initiate Phase 2 development in oral and IV formulations in 2027, subject to regulatory agreement, after completing the Phase 1 study of intravenous SCY-247 (October 22, 2026). Exact day not announced.Estimated windowPrimary source
H2 2027$SGMTSagimet Biosciences Inc.Topline results from AURORA, the pivotal U.S. Phase 3 trial of denifanstat in moderate to severe acne, expected in the second half of 2027 according to the company. Exact day not announced.Estimated windowPrimary source
2027$SNDXSYNDAX PHARMACEUTICALS INCIND submission: SNDX-62122 · Myelofibrosis. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$SNDXSYNDAX PHARMACEUTICALS INCInitial data: Revuforj (revumenib) · myelofibrosis (MF) (Phase 1/2). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$SRZNSurrozenInitial DUET Phase 1b/2a data expected H2 2027 per company guidance. Exact event day is not announced.Estimated windowPrimary source
H2 2027$STOKStoke Therapeutics, Inc.Zorevunersen NDA completion planned H2 2027 after Q3 2027 EMPEROR topline, subject to supporting data. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$SUPNSUPERNUS PHARMACEUTICALS INCPotential FDA authorization of a second supplier for ONAPGO. This concerns manufacturing supply for an already approved treatment, not initial marketing approval. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
2027$SYRESPYRE THERAPEUTICS INCTopline data: SPY001, SPY002, SPY003, SPY120, SPY130, SPY230 · Ulcerative colitis (UC) (Phase 2). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$TARSTARSUS PHARMACEUTICALS INCRegulatory decision: XDEMVY (lotilaner ophthalmic solution) · Demodex blepharitis. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$TRAXFIRST TRACKS BIOTHERAPEUTICS INCFirst Tracks plans to initiate a late-stage ANB033 trial in celiac disease in 2027. Exact timing and the trial phase are not specified in the October 12 release.Estimated windowCompany release
H2 2027$TRVITREVI THERAPEUTICS INCTopline data: Haduvio (oral nalbuphine ER) · idiopathic pulmonary fibrosis (IPF)-related chronic cough, OCEAN-2 (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$TRVITREVI THERAPEUTICS INCTopline data: Haduvio (oral nalbuphine ER) · Refractory chronic cough; IPF-related chronic cough; non-IPF ILD-related chronic cough (Phase 2b). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 guidance; exact day unspecified$TTRXTurn Therapeutics Inc.GX-03 atopic dermatitis Phase 3 initiation planned in 2027, described as mid-2027 in the pipeline slide. Conditional on preceding development and funding. Company guidance; no exact event day announced.Estimated windowPrimary source
2027$TVTXTRAVERE THERAPEUTICS INCConference presentation: FILSPARI (sparsentan) · recurrent IgAN or FSGS. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$TVTXTRAVERE THERAPEUTICS INCTopline data: pegtibatinase · classical Homocystinuria (HCU) (Phase 3). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
2027$TYRATYRA BIOSCIENCES INCInitial data: oral dabogratinib · FGFR3-altered low-grade upper tract urothelial carcinoma (LG-UTUC) (Phase 2a/b). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Mid-2027 (approximate)$VCREVICORE PHARMA HOLDING ABTopline data: buloxibutid · IPF. Company timing: Mid-2027 (approximate). Exact event day is not announced.Estimated windowPrimary source
Supporting source
2027$VERAVERA THERAPEUTICS INCRegulatory decision: atacicept · IgA nephropathy (IgAN) (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$VIRVir Biotechnology, Inc.Vir and Astellas anticipate starting pivotal Phase 3 trials of VIR-5500 in prostate cancer in 2027, without a specified quarter. Company guidance; no exact event day.Estimated windowPrimary source
2027$VKTXViking TherapeuticsResults of Part 2 maintenance dosing in obesity expected during 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$VSTMVerastem, Inc.Initial data from the Phase 2 TARGET-D 202 (second-line NSCLC) and TARGET-D 203 (second-line colorectal cancer) trials of VS-7375, expected in the second half of 2027. Company guidance; no date announced.Estimated windowSEC filing
2027$XENEXENON PHARMACEUTICALS INCInitial data: NBI-921355 · Certain types of epilepsy (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
H2 2027$XNCRXENCOR INCTopline data: XmAb942 (Xtend TL1A) · ulcerative colitis (UC) (Phase 2b). Company timing: H2 2027. Exact event day is not announced.Estimated windowPrimary source
2027$XNCRXENCOR INCPhase 1 combination dose escalation of XmAb541 and XmAb808 is expected to reach its target dose range in 2027. No dated interim-data disclosure is specified. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$ZBIOZENAS BIOPHARMA INCZB022: Phase 1 initiation for the oral, brain-penetrant TYK2-JH2 inhibitor is expected in 2027, subject to IND-enabling study results and regulatory clearance. This replaces the earlier 2026 plan. Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
2027$ZLABZAI LAB LTDTopline data: elegrobart · thyroid eye disease (TED) (Phase 3). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
2027$ZLABZAI LAB LTDIND submission: ZL-1222 (PD-1 / IL-12) (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
ZLAB stock hub
2027$ZYMEZYMEWORKS INCIND submission: ZW1528 · chronic obstructive pulmonary disease (COPD) (Phase 1). Company timing: 2027. Exact event day is not announced.Estimated windowPrimary source
Approximately November 2027-January 2028 (18-20 months from May 11, 2026)$HROWHARROW INCFDA filing planned for the TRIESENCE prefilled-syringe format within 18-20 months of the May 11, 2026 update. This corresponds approximately to November 2027-January 2028 and is separate from the cataract-surgery/pain clinical study. Company timing: Approximately November 2027-January 2028 (18-20 months from May 11, 2026). Exact event day is not announced.Estimated windowPrimary source
Q1 2028$LBRXLB PHARMACEUTICALS INCTopline data: LB-102 · Bipolar depression, ILLUMINATE-1 (Phase 2). Company timing: Q1 2028. Exact event day is not announced.Estimated windowPrimary source
Q1 2028$OCULOCULAR THERAPEUTIX INCTopline data: AXPAXLI · wet AMD (nAMD), SOL-R (Phase 3). Company timing: Q1 2028. Exact event day is not announced.Estimated windowPrimary source
Early 2028$PALIPalisade Bio, Inc.ASCENTRA-CD Crohn's Phase 2 primary efficacy readout. Estimated window: early 2028. Exact event day is not announced.Estimated windowPrimary source
Q1 2028$QNCXIRulya Therapeutics Inc. (formerly Quince Therapeutics)LAM-001 Phase 2b data in pulmonary hypertension associated with interstitial lung disease expected Q1 2028. Company guidance, not a confirmed day. IRulya is the current company name; QNCX changes to IRLA on October 12, 2026.Estimated windowPrimary source
H1 2028$HROWHARROW INCG-MELT: potential FDA approval in H1 2028 under the company development plan, following the intended H1 2027 NDA submission. This is a conditional forecast, not an assigned PDUFA deadline; potential launch is a separate H2 2028 milestone. Company timing: H1 2028. Exact event day is not announced.Estimated windowPrimary source
H1 2028$NGENNervGenNervGen expects RESTORE Phase 3 topline results in H1 2028 in chronic cervical motor-incomplete spinal cord injury.Estimated windowCompany release
Trial registry
H1 2028$PCSAProcessa Pharmaceuticals, Inc.VT7208 proof-of-concept data in chronic spontaneous urticaria planned for H1 2028. Company guidance in the October 5 SEC disclosure; the disclosure date is not necessarily the first announcement of this plan. Exact event day is not announced.Estimated windowPrimary source
H1 2028$PCVXVAXCYTE INCVAX-31 adult BLA submission planned in H1 2028, subject to supporting development data; company guidance, not an FDA-confirmed date. Exact event day is not announced.Estimated windowPrimary source
Early 2028$SNDXSYNDAX PHARMACEUTICALS INCTopline data: axatilimab · chronic graft-versus-host disease (GVHD) (Phase 3). Company timing: Early 2028. Exact event day is not announced.Estimated windowPrimary source
Early 2028$STOKSTOKE THERAPEUTICS INCPotential US approval and launch targeted in early 2028, conditional on supporting data, NDA submission and FDA review. Not a confirmed FDA deadline. Exact event day is not announced.Estimated windowPrimary source
Late 2027 / early 2028$SYRESPYRE THERAPEUTICS INCClinical data readout: SPY072 + IL-17A/F · HS. Company timing: Late 2027 / early 2028. Exact event day is not announced.Estimated windowPrimary source
H1 2028$TRVITREVI THERAPEUTICS INCTopline data: Haduvio (oral nalbuphine ER) · idiopathic pulmonary fibrosis (IPF)-related chronic cough, OCEAN-1 (Phase 3). Company timing: H1 2028. Exact event day is not announced.Estimated windowPrimary source
H1 2028$TTRXTurn Therapeutics Inc.GX-03 onychomycosis Phase 3 interim analysis guided to H1 2028, conditional on trial execution and funding. The presentation conflicts on initiation timing (Q1 versus Q2 2027); no start date has been confirmed. Company guidance; no exact event day announced.Estimated windowPrimary source
Late 2027 / early 2028$ZYMEZYMEWORKS INCTopline data: EmpowHER-303 HER-303. Company timing: Late 2027 / early 2028. Exact event day is not announced.Estimated windowPrimary source
2028$ANABANAPTYSBIO INCTopline data: Jemperli (dostarlimab) · colorectal cancer (CRC) and dMMR pan tumors (Phase 3). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
ANAB stock hub
Late 2028$CELCCELCUITY INCTopline data: REVTORPYK (gedatolisib) · endocrine-resistant HR+/HER2- ABC (Phase 3). Company timing: Late 2028. Exact event day is not announced.Estimated windowPrimary source
H2 2028$DNTHDIANTHUS THERAPEUTICS INCTopline data: claseprubart · Generalized myasthenia gravis (gMG), EMERGE (Phase 3). Company timing: H2 2028. Exact event day is not announced.Estimated windowPrimary source
H2 2028$GPCRSTRUCTURE THERAPEUTICS INCTopline data: aleniglipron · chronic weight management, ACCOMPLISH-1 and ACCOMPLISH-2 (Phase 3). Company timing: H2 2028. Exact event day is not announced.Estimated windowPrimary source
2028$HCMHUTCHMED (CHINA) LTDInitial data: IMG-007 · Alopecia areata (Phase II). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
2028$HELPCybin Inc. doing business as Helus PharmaHLP003 (adjunctive treatment of major depressive disorder): Helus Pharma expects to file a New Drug Application with the FDA in 2028. Exact day not announced; a planned filing is not FDA acceptance or approval.Estimated windowPrimary source
2028$HRMYHARMONY BIOSCIENCES HOLDINGS INCPotential regulatory decision (company forecast): WAKIX (pitolisant) (Phase 3). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
2028$HRMYHARMONY BIOSCIENCES HOLDINGS INCPotential regulatory decision (company forecast): Pitolisant HD · Narcolepsy. Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
2028$HRMYHARMONY BIOSCIENCES HOLDINGS INCPotential regulatory decision (company forecast): EPX-100 (clemizole hydrochloride) · Dravet syndrome (DS) and Lennox-Gastaut syndrome; rare epilepsies (Phase 3). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
2028$IMVTIMMUNOVANT INCTopline data: imeroprubart (IMVT-1402) · Sjögren's disease (potentially registrational). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2028$IMVTIMMUNOVANT INCTopline data: imeroprubart (IMVT-1402) · chronic inflammatory demyelinating polyneuropathy (CIDP) (potentially registrational). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
Trial registry
2028$KLRAKAILERA THERAPEUTICS INCClinical data readout: ribupatide injection (KAI-9531) · Obesity (Phase 3). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
2028$LGNDLIGAND PHARMACEUTICALS INCClinical data readout: Qarziba · Neuroblastoma, BEACON-2. Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
Mid-2028 (approximate)$NKTRNEKTAR THERAPEUTICSClinical data readout: rezpegaldesleukin (Phase 3). Company timing: Mid-2028 (approximate). Exact event day is not announced.Estimated windowPrimary source
H2 2028$PCSAProcessa Pharmaceuticals, Inc.VT7208 proof-of-concept data in relapsing multiple sclerosis planned for H2 2028, per company guidance disclosed in an October 5 SEC filing. Exact event day is not announced.Estimated windowPrimary source
Q4 2028$QNCXIRulya Therapeutics Inc. (formerly Quince Therapeutics)LAM-001 Phase 2 data in sarcoidosis-associated pulmonary hypertension expected Q4 2028. Company guidance, not a confirmed day. IRulya is the current company name; QNCX changes to IRLA on October 12, 2026.Estimated windowPrimary source
Mid-2028; exact range unspecified$RCKTRocket Pharmaceuticals, Inc.Rocket guides pivotal Danon Phase 2 topline to mid-2028. No exact day or quarter has been given. Exact event day is not announced.Estimated windowPrimary source
2028$TARSTARSUS PHARMACEUTICALS INCTopline data: aqueous chlorine dioxide solution (IRX-101) COMFORT (Phase 3). Company timing: 2028. Exact event day is not announced.Estimated windowPrimary source
Q4 2028$TTRXTurn Therapeutics Inc.GX-03 onychomycosis Phase 3 topline guided to Q4 2028, conditional on execution and funding. Initiation timing remains inconsistent across issuer slides. Company guidance; no exact event day.Estimated windowPrimary source
Late 2028$XERSXERIS BIOPHARMA HOLDINGS INCXP-8121: topline results from the Cornerstone Phase 3 program in hypothyroidism are forecast for late 2028. This is a company development projection. Company timing: Late 2028. Exact event day is not announced.Estimated windowPrimary source
Early 2029$ATAIATAIBECKLEY INCTopline data: BPL-003 (Phase 3). Company timing: Early 2029. Exact event day is not announced.Estimated windowPrimary source
H1 2029$LBRXLB PHARMACEUTICALS INCTopline data: LB-102 · adjunctive treatment of MDD (Phase 2). Company timing: H1 2029. Exact event day is not announced.Estimated windowPrimary source
2029$NKTRNEKTAR THERAPEUTICSTarget for the first rezpegaldesleukin BLA submission. This is company development guidance, not a scheduled FDA approval decision. Company timing: 2029. Exact event day is not announced.Estimated windowPrimary source
2029$NUVBNUVATION BIO INCClinical data readout: safusidenib · IDH1-mutant astrocytoma (pivotal Phase 3). Company timing: 2029. Exact event day is not announced.Estimated windowPrimary source
H2 2029$TARSTARSUS PHARMACEUTICALS INCTopline data: gildeuretinol (ALK-001) · Stargardt disease (Phase 3). Company timing: H2 2029. Exact event day is not announced.Estimated windowPrimary source
2030$CELCCELCUITY INCTopline data: REVTORPYK (gedatolisib) · endocrine-sensitive HR+/HER2- ABC (Phase 3). Company timing: 2030. Exact event day is not announced.Estimated windowPrimary source
2030$REPLREPLIMUNE GROUP INCRP1 (vusolimogene oderparepvec) plus nivolumab: primary overall-survival readout from Phase 3 IGNYTE-3 is expected in 2030. The trial compares the combination with physician's choice in advanced melanoma after anti-PD-1 and anti-CTLA-4 therapies or when anti-CTLA-4 is unsuitable. The H2 2027 interim OS analysis is a separate milestone. Company timing: 2030. Exact event day is not announced.Estimated windowPrimary source
2030$XERSXERIS BIOPHARMA HOLDINGS INCXP-8121: potential FDA approval and commercial launch in 2030 are long-range company projections, conditional on trial outcomes and regulatory review; no assigned PDUFA date. Company timing: 2030. Exact event day is not announced.Estimated windowPrimary source
Supporting source

Recent history: 223 events

The following rows record completed events and dates that have passed. A past date does not prove an outcome or that a scheduled presentation occurred; uncertain status is stated in each row.

Date / windowTickerCompanyEventStatusSources
2026-10-22$VERAVera Therapeutics, Inc.The ORIGIN 3 final efficacy analysis of TRUTAKNA (atacicept-vymj) in adults with primary IgA nephropathy was presented on October 22, 2026 as a featured late-breaking oral in the opening plenary of ASN Kidney Week 2026 and published the same day in The New England Journal of Medicine. According to the company, TRUTAKNA achieved statistical significance on all prespecified endpoints, including eGFR change from baseline and annualized slope and risk reduction in composite kidney disease progression events. Adverse events occurred in 160/214 patients (75%) on TRUTAKNA and 167/214 (78%) on placebo; serious adverse events in 7% versus 15%. Vera plans to submit the supplemental BLA in Q4 2026, with potential full approval expected in 2027.HISTORICAL · Disclosed eventPrimary source
Supporting source
2026-10-22$SGMTSagimet Biosciences Inc.Sagimet announced that the first patient has been dosed in AURORA (NCT07863193), its pivotal U.S. Phase 3 trial of once-daily oral denifanstat 50 mg in moderate to severe acne. The randomized, double-blind, placebo-controlled trial is designed to enroll approximately 800 patients aged 12 and older, about 450 of them adolescents, with a 12-week double-blind period followed by a 40-week open-label extension; it is intended to support a potential U.S. NDA. Topline results are expected in the second half of 2027.HISTORICAL · Disclosed eventPrimary source
2026-10-22$OCSOculis Holding AGOculis released on October 22, 2026 the late-breaking Phase 2 ACUITY biomarker data on privosegtor in optic neuritis presented at the 10th Joint ACTRIMS-ECTRIMS Meeting (MSToronto 2026). Increases in plasma neurofilament light chain (NfL) and glial fibrillary acidic protein (GFAP) were reduced with privosegtor versus placebo, particularly at early timepoints after acute onset: at Day 5 the mean increases in both markers were higher in the placebo group; NfL remained stable in the privosegtor group through Month 6, and GFAP remained below baseline in the privosegtor group from Month 1 through Month 6 while it stayed above baseline with placebo. The company presents these as biomarker findings complementing the previously reported visual and retinal results.HISTORICAL · Disclosed eventPrimary source
Supporting source
2026-10-22$CGTXCognition Therapeutics, Inc.Cognition Therapeutics announced alignment with the FDA on key elements of a pivotal Phase 3 study of zervimesine (CT1812) in dementia with Lewy bodies, including patient selection, dose, duration and endpoints. The planned registrational study is expected to enroll participants with mild-to-moderate DLB randomized to 100 mg once-daily oral zervimesine or placebo for nine months; the primary endpoint will be the NPI-2 measure of hallucinations and delusions, with ADCS-ADL as a key secondary endpoint. The company is completing the protocol; no start date was announced.HISTORICAL · Disclosed eventPrimary source
2026-10-22$ABUSArbutus Biopharma CorporationArbutus announced that the FDA notified the company that the clinical hold on the IND application for AB-101, its oral PD-L1 inhibitor for chronic hepatitis B, has been removed and that it may engage in additional clinical development of AB-101 in the United States. The company is evaluating next steps for the program.HISTORICAL · Disclosed eventPrimary source
October 17–21, 2026; ePoster day unspecified$TLXTelix Pharmaceuticals LimitedEANM 2026, 39th Annual Congress of the European Association of Nuclear Medicine (Vienna, October 17–21, 2026): ePoster EP-0460 with preliminary results from the Phase 3 trial of TLX591-Px (68Ga-PSMA-11; Illuccix) PET for detection of biochemical recurrence of prostate cancer in Chinese men (NCT05847348). The company release does not specify the ePoster day.HISTORICAL · Outcome unverifiedPrimary source
Supporting source
October 20–21, 2026$SVRASavara Inc.CHEST 2026 (Phoenix): rapid-fire oral on long-term efficacy and safety of molgramostim in autoimmune pulmonary alveolar proteinosis from the IMPALA-2 open-label period on October 20, and a poster on patients with mild diffusion impairment on October 21. Encore and new analyses, not a new pivotal readout. The FDA target action date for the BLA is November 22, 2026.HISTORICAL · Outcome unverifiedPrimary source
Supporting source
2026-10-21$SUPNSupernus Pharmaceuticals, Inc.Supernus announced that the FDA has recognized seven years of orphan-drug market exclusivity for ONAPGO (apomorphine HCl) for the treatment of motor fluctuations in adults with advanced Parkinson's disease. The seven-year exclusivity period began on February 3, 2025, the date of FDA approval. Separately, the company has submitted a supplemental NDA (sNDA) for a second manufacturing supplier for ONAPGO and continues to expect potential FDA approval of the second supplier by mid-year 2027 (unchanged from prior guidance).HISTORICAL · Disclosed eventPrimary source
2026-10-21$ROIVRoivant Sciences Ltd.Roivant and its subsidiary Priovant Therapeutics announced positive topline results from the Phase 3 CLARITY-1 and CLARITY-2 trials of brepocitinib in non-infectious uveitis (NIU). Primary endpoint (time to treatment failure, assessed weeks 6-48) met with high statistical significance in both studies (p<0.0001). CLARITY-1 (n=166): hazard ratio 0.27 (95% CI 0.17-0.43); cumulative failure incidence at week 48 of 35.4% with brepocitinib versus 78.7% with placebo. CLARITY-2 (n=204): hazard ratio 0.22 (95% CI 0.14-0.34); cumulative failure incidence at week 48 of 32.4% versus 77.8%. Median time to treatment failure exceeded 48 weeks with brepocitinib versus approximately 12 weeks with placebo in both studies. Pooled steroid-free quiescence at week 48: 62% with brepocitinib versus 20% with placebo (p<0.0001). Key secondary endpoints (angiographic response, macular edema resolution, patient-reported visual function) also reached statistical significance. Safety data were consistent with prior brepocitinib clinical trials; no new safety signals. Brepocitinib is already approved in the U.S. for dermatomyositis under the brand name LISRAYA. Priovant intends to file a supplemental NDA for brepocitinib in NIU in the first half of calendar year 2027.HISTORICAL · Disclosed eventSEC filing
SEC filing
October 21, 2026$KYTXKyverna Therapeutics, Inc.KYSA-8 Phase 2 miv-cel full one-year dataset in stiff person syndrome: MSToronto poster P0364, October 21, 4:30–6:30 p.m. ET. Presentation of follow-up data; the September 24 topline remains a separate historical event.HISTORICAL · Outcome unverifiedPrimary source
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2026-10-21$CRDFCardiff Oncology, Inc.The FDA granted Orphan Drug Designation to onvansertib, Cardiff Oncology's oral PLK1 inhibitor, for the treatment of chronic myelomonocytic leukemia (CMML). Early investigator-initiated Phase 1 data presented at ASH 2025 showed preliminary efficacy in RAS-pathway-mutated CMML patients (40-50% of the myeloproliferative subtype), including a 100% platelet response, white blood cell normalization, a splenic response and a reduction in marrow blasts from 8% to 2% that enabled an allogeneic stem cell transplant in one patient. Onvansertib's lead program remains a planned registration-enabling first-line study in RAS-mutated metastatic colorectal cancer (mCRC) at the 30 mg dose, in combination with FOLFIRI/bevacizumab.HISTORICAL · Disclosed eventPrimary source
2026-10-21$CRDFCardiff Oncology, Inc.The FDA granted Orphan Drug Designation to onvansertib, Cardiff Oncology's oral PLK1 inhibitor, for the treatment of chronic myelomonocytic leukemia (CMML). Early investigator-initiated Phase 1 data presented at ASH 2025 showed preliminary efficacy in RAS-pathway-mutated CMML patients (40-50% of the myeloproliferative subtype), including a 100% platelet response, white blood cell normalization, a splenic response and a reduction in marrow blasts from 8% to 2% that enabled an allogeneic stem cell transplant in one patient. Onvansertib's lead program remains a planned registration-enabling first-line study in RAS-mutated metastatic colorectal cancer (mCRC) at the 30 mg dose, in combination with FOLFIRI/bevacizumab.HISTORICAL · Disclosed eventPrimary source
2026-10-21$TGTXTG Therapeutics, Inc.TG Therapeutics released its MSToronto2026 posters on October 21, 2026, including seven-year ULTIMATE I/II follow-up and an ENABLE real-world update for BRIUMVI (ublituximab-xiiy) in relapsing MS. At seven years, 88.3% of patients on continuous BRIUMVI treatment remained free from 24-week confirmed disability progression; 11.7% progressed versus 17.4% in the switch group, patients who initially received teriflunomide before switching to BRIUMVI (p=0.0148), and 17.6% achieved confirmed disability improvement versus 13.6% in the switch group (p=0.0492). This comparison is not randomized and the p-values are nominal. The annualized relapse rate in Year 7 was 0.018, and the company reported no apparent increase in exposure-adjusted adverse event rates over time. In the Phase 4 observational ENABLE study (updated analysis of 1,076 participants), 99.2% remained relapse-free during treatment (ARR 0.014) and first-dose infusion-related reactions occurred in 18.8%.HISTORICAL · Disclosed eventPrimary source
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2026-10-21$TGTXTG Therapeutics, Inc.Phase 3 ENHANCE data on a single BRIUMVI initiation dose were released with the MSToronto2026 posters on October 21, 2026, ahead of the October 22 poster session. The trial met its primary endpoint, demonstrating bioequivalent drug exposure between the approved initiation regimen (150 mg on Day 1 and 450 mg on Day 15) and a consolidated single 600 mg infusion on Day 1, eliminating the need for a Day 15 infusion. Infusion-related reactions were comparable between regimens and lower than those reported in the ULTIMATE studies, with no Grade 3 or higher reactions in any participant. The company describes the single-dose initiation schedule as proposed.HISTORICAL · Disclosed eventPrimary source
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2026-10-21$TGTXTG Therapeutics, Inc.TG Therapeutics released its MSToronto2026 ePoster data on October 21, 2026. Phase 1 pharmacokinetics: subcutaneous BRIUMVI showed mean bioavailability above 60% relative to IV, and the company says PK modeling and simulation informed by these data support the quarterly subcutaneous regimen being evaluated in its fully enrolled Phase 3 trial, whose topline remains a separate future event. Switching analyses in the ENHANCE study: among participants who reported wearing-off on ocrelizumab, switching to BRIUMVI was associated with a 69% reduction in reported wearing-off at Week 24, sustained through Week 48; among participants not B-cell depleted when switching from a prior anti-CD20 antibody, 100% achieved B-cell depletion at Week 24 and 92.6% remained depleted at Week 48. BRILL, a non-interventional real-world study sponsored by Neuraxpharm (48-week interim analysis of 169 patients): the proportion of patients with a relapse decreased by 93% versus the 12 months before starting BRIUMVI, with an on-treatment ARR of 0.05.HISTORICAL · Disclosed eventPrimary source
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early 2027$NKTRNektar TherapeuticsPlanned registrational Phase 3 rezpegaldesleukin study initiation in alopecia areata, expected in early 2027 (company guidance of August 13, 2026). Replaced by the ZENITH AA entry after the company's October 1, 2026 release.HISTORICAL · Superseded estimateSEC filing
2026-10-21$IMUXImmunic, Inc.MSToronto2026 poster P0387 (Poster Session 1, October 21, 2026, 4:30–6:30 p.m. ET), disclosed by the company on October 21: in the open-label extension of the Phase 2 CALLIPER trial in progressive MS, the favorable trends on disability outcomes seen in the double-blind period were maintained among participants who continued vidofludimus calcium; 6.5% of patients discontinued through the January 27, 2026 data cutoff, and safety and tolerability appeared consistent with the double-blind period. Among the 387 participants who entered the extension, 44.4% had at least one treatment-emergent adverse event and 5.7% a serious one. CALLIPER did not meet its primary endpoint of percent brain volume change.HISTORICAL · Disclosed eventPrimary source
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2026-10-21$IMUXImmunic, Inc.MSToronto2026 ePosters EP2473 and EP2205 (on display for the duration of the congress), disclosed by the company on October 21, 2026. Exploratory CALLIPER analysis: vidofludimus calcium reduced EBV-specific T-cell receptor (TRB) sequence matches versus placebo (-0.65; p=0.0004), with influenza A-specific matches unchanged (+0.08; p=0.5983); in a post-hoc analysis, reductions were associated with improved SDMT scores. Post-hoc analysis with proposed bidirectional disability measures: 2.47 times higher likelihood of 24-week confirmed disability improvement (nominal p=0.037), positive confirmed disability change (nominal p=0.042), and 1.5 times higher likelihood of a better outcome by generalized pairwise comparisons (p=0.042). Exploratory and post-hoc analyses of a Phase 2 trial that missed its primary endpoint.HISTORICAL · Disclosed eventPrimary source
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2026-10-21$BCRXBioCryst Pharmaceuticals, Inc.The FDA approved BioCryst's sNDA for the 150 mg oral pellet formulation of once-daily ORLADEYO (berotralstat) for prophylaxis to prevent attacks of hereditary angioedema in adults and adolescents aged 12 years and older, announced October 21, 2026. Patients can now take ORLADEYO in capsule or pellet form; the pellet formulation had been approved in December 2025 for patients aged 2 to under 12. The approval was based on chemistry, manufacturing and controls information and on data showing the safety and tolerability of the pellets compared with the capsules.HISTORICAL · Disclosed eventFinviz (news)
2026-10-20$VCREVICORE PHARMA HOLDING ABVicore Pharma's CEO takes part in a panel at the Chardan Healthcare Conference in New York on October 20, 2026, 2:00–2:30 p.m. ET. An investor conference appearance, not a data release.HISTORICAL · Outcome unverifiedPrimary source
2026-10-20$RCUSARCUS BIOSCIENCES INCArcus Biosciences disclosed new data from the ARC-20 platform study of casdatifan in clear cell renal cell carcinoma (ccRCC), data cutoff September 4, 2026. In second-line combination with cabozantinib (n=43, median follow-up 21.3 months): median progression-free survival 14.5 months, 18-month landmark overall survival 77%, confirmed objective response rate 44%. In a late-line monotherapy cohort pooling patients with one, two or three prior TKI-based therapies (n=121): median overall survival 35 months, median progression-free survival 13 months, confirmed objective response rate 36%. No unexpected safety signals were observed at the data cutoff. The release reports response, PFS and OS by cohort without a stated primary endpoint or a placebo/active comparator.HISTORICAL · Disclosed eventSEC filing
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2026-10-20$RCUSARCUS BIOSCIENCES INCArcus Biosciences disclosed new data from the ARC-20 platform study of casdatifan in clear cell renal cell carcinoma (ccRCC), data cutoff September 4, 2026. In second-line combination with cabozantinib (n=43, median follow-up 21.3 months): median progression-free survival 14.5 months, 18-month landmark overall survival 77%, confirmed objective response rate 44%. In a late-line monotherapy cohort pooling patients with one, two or three prior TKI-based therapies (n=121): median overall survival 35 months, median progression-free survival 13 months, confirmed objective response rate 36%. No unexpected safety signals were observed at the data cutoff. The release reports response, PFS and OS by cohort without a stated primary endpoint or a placebo/active comparator.HISTORICAL · Disclosed eventSEC filing
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2026-10-20$IONSIONIS PHARMACEUTICALS INCThe FDA approved Hibsago (bepirovirsen), an antisense oligonucleotide GSK licensed from Ionis in 2019, for chronic hepatitis B in combination with nucleos(t)ide analogue reverse-transcriptase inhibitor (NrtI) therapy, announced October 20, 2026, ahead of the October 26, 2026 PDUFA date. Indication: adults without cirrhosis on NrtI therapy for at least 6 months, with suppressed HBV DNA and HBsAg ≤3,000 IU/mL by an FDA-authorized test. Treatment course is six months, with home administration possible after the first dose. In the pooled Phase 3 B-Well 1/2 data, 19% of participants (233 of 1,220) achieved functional cure — undetectable HBV DNA and HBsAg sustained for at least 24 weeks after stopping all treatment — versus 0% on placebo (0 of 614); the rate was 26% in the subgroup with baseline HBsAg ≤1,000 IU/mL. Labeled warnings include hepatic flares and thrombocytopenia, contraindicated below 100 x 10^9 platelets/L.HISTORICAL · Disclosed eventPrimary source
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2026-10-20$HCMHutchmedHUTCHMED's exclusive development and license agreement with a GSK subsidiary for HMPL-A830, a KRAS-EGFR antibody-targeted therapy conjugate (ATTC), closed on October 20, 2026, after customary closing conditions including antitrust review, following the agreement first announced September 3, 2026. The GSK subsidiary receives rights to develop and commercialize HMPL-A830 worldwide excluding mainland China, Hong Kong, Macau and Taiwan; HUTCHMED remains responsible for the global Phase Ia development program, initiated in September 2026 (NCT07718581). HUTCHMED expects to receive a $110 million upfront payment shortly, with up to $1.185 billion in additional development, regulatory and commercial milestones, plus tiered royalties on net sales.HISTORICAL · Disclosed eventFinviz (news)
2026-10-20$AAPGASCENTAGE PHARMA GROUP INTERNATIONALChina's Center for Drug Evaluation (CDE), under the National Medical Products Administration (NMPA), granted Breakthrough Therapy Designation to Ascentage Pharma's lisaftoclax (APG-2575), the company's Bcl-2 inhibitor, in combination with acalabrutinib, for treatment-naive adult patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL), announced October 20, 2026. Lisaftoclax was previously approved in China in July 2025 for CLL/SLL patients who had received at least one prior systemic therapy including a BTK inhibitor; the new designation applies specifically to the first-line combination evaluated in the global registrational Phase III trial GLORA-2. In the United States, lisaftoclax remains investigational and has not been approved by the FDA; the combination with acalabrutinib is investigational and not approved in any market.HISTORICAL · Disclosed eventPrimary source
October 20, 2026$RGNXREGENXBIO Inc.Sura-vec wet-AMD investor event on October 20, 1–4 p.m. ET, with clinical-program and retina-specialist discussion. The separate ATMOSPHERE/ASCENT pivotal topline remains guided for Q4 2026; this event is not the announced readout.HISTORICAL · Outcome unverifiedPrimary source
2026-10-20$IRDOpus Genetics, Inc.Opus Genetics presents at the Chardan Annual Healthcare Conference on Tuesday, October 20, 2026, at 10:00 a.m. ET, with a live and archived webcast. An investor conference appearance, not a data release.HISTORICAL · Outcome unverifiedPrimary source
2026-10-20$APMDApnimed, Inc.CHEST 2026 (Phoenix, October 18–21): two late-breaking AD109 abstracts in obstructive sleep apnea on October 20, a rapid-fire oral on post-menopausal women and a poster on baseline hypoxic burden and blood-pressure response, plus a CHEST panel on the Phase 3 SynAIRgy and LunAIRo results. Analyses of already reported Phase 3 trials, not a new pivotal readout.HISTORICAL · Outcome unverifiedPrimary source
2026-10-20$ANABAnaptysBioPost-trial hearing in GSK/Tesaro Jemperli litigation. Hearing date is not judgment date.HISTORICAL · Outcome unverifiedSEC filing
UEG Week 2026-10-17–2026-10-20$ABVXABIVAX SAConference presentation: obefazimod. Company timing: UEG Week 2026-10-17–2026-10-20. Congress: UEG Week. The conference range does not establish the individual presentation day.HISTORICAL · Outcome unverifiedSEC filing
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2026-10-20$RAPPRAPPORT THERAPEUTICS INCTopline data announced: RAP-219 · acute bipolar mania (Phase 2, 253 adults). Primary endpoint met: 3.1-point placebo-adjusted improvement in YMRS total score at week 3 (p=0.045); secondary CGI-BP mania severity met (0.4 points, p=0.024). No serious adverse events during treatment; treatment discontinuation 24.6% on RAP-219 vs 11.8% on placebo. End-of-Phase 2 FDA meeting expected Q1 2027; two Phase 3 trials expected to start in H2 2027.HISTORICAL · Disclosed eventSEC filing
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2026-10-19$SYRESpyre Therapeutics, Inc.UEGW 2026 (Barcelona) moderated poster on Monday, October 19, 16:06-16:12 CEST (New Insights into IBD Biology (II), Hall 7, Poster Stage 2, presenter Andy Spencer): preclinical data in TNBS-induced colitis in humanized mice showing that anti-α4β7, anti-TL1A and anti-IL-23 are efficacious and that combinations further improve efficacy. Preclinical data, not a clinical readout.HISTORICAL · Outcome unverifiedPrimary source
2026-10-19$SLNSilence Therapeutics plcMerck KGaA, Darmstadt, Germany, agrees to acquire Silence Therapeutics plc for $20.00 per ADS in cash (three ordinary shares per ADS), valuing the company at approximately $1.3 billion in equity value and $1.1 billion in enterprise value — a 130% premium to the October 16, 2026 close and an 82% premium to the 30-day volume-weighted average price of $10.99. Structured as a UK scheme of arrangement under Part 26 of the Companies Act 2006, unanimously approved by Silence's board; holders of about 14% of voting rights have signed a voting and support agreement in favor of the transaction. Closing is subject to shareholder approval, sanction by the High Court of Justice of England and Wales, and customary regulatory approvals, expected to complete in Q1 2027.HISTORICAL · Disclosed eventSEC filing
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2026-10-19$SLNSilence Therapeutics plcMerck KGaA, Darmstadt, Germany, agrees to acquire Silence Therapeutics plc for $20.00 per ADS in cash (three ordinary shares per ADS), valuing the company at approximately $1.3 billion in equity value and $1.1 billion in enterprise value — a 130% premium to the October 16, 2026 close and an 82% premium to the 30-day volume-weighted average price of $10.99. Structured as a UK scheme of arrangement under Part 26 of the Companies Act 2006, unanimously approved by Silence's board; holders of about 14% of voting rights have signed a voting and support agreement in favor of the transaction. Closing is subject to shareholder approval, sanction by the High Court of Justice of England and Wales, and customary regulatory approvals, expected to complete in Q1 2027.HISTORICAL · Disclosed eventSEC filing
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2026-10-19$LLYEli Lilly and CompanyLilly reports one-year Phase 3 SHINE-2 results for Omvoh (mirikizumab-mrkz) in pediatric ulcerative colitis: the trial met its primary endpoint, with 50% of Week-12 responders (n=52 of 63 enrolled patients aged 4-17) in clinical remission at Week 52. Lilly describes it as the first IL-23p19 inhibitor to report one-year Phase 3 data in this pediatric population. Safety through Week 52 was consistent with the known adult profile, with no new signals; serious adverse events in 6.3% of patients, none treatment-related; no deaths, malignancies, opportunistic infections or growth issues reported.HISTORICAL · Disclosed eventPrimary source
2026-10-19$GSKGSK plcFDA grants accelerated approval to Jemperli (dostarlimab) monotherapy for adults with stage II/III dMMR/MSI-H locally advanced rectal cancer, based on the single-arm Phase 2 AZUR-1 study: 68% sustained clinical complete response at 12 months in the investigator assessment (98/144 evaluable patients); 47% in the independent central review (54/116), data still maturing. First and only immunotherapy approved in the US for this indication; accelerated approval, continued approval may depend on a confirmatory trial. Serious adverse reactions in 20% of patients. Full AZUR-1 interim data to be presented at ESMO 2026. Sources: SEC 6-K and company press release.HISTORICAL · Disclosed eventSEC filing
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October 19, 2026$EPRXEupraxia Pharmaceuticals Inc.UEG oral abstract: histopathological changes in eosinophilic esophagitis after a single EP-104GI administration during Phase 1b/2 RESOLVE dose escalation, October 19. Separate endpoint from dysphagia posters; not randomized Phase 2b interim data.HISTORICAL · Outcome unverifiedPrimary source
2026-10-19$TLXTelix Pharmaceuticals LimitedEANM 2026, 39th Annual Congress of the European Association of Nuclear Medicine (Vienna), October 19, 2026, 16:45–18:15 CEST: oral presentation (abstract OP-523, presenter Yehia Omar, Misr Radiology) of interim results from the PTherpan-Lu trial of TLX597-Tx ([177Lu]Lu-panPSMA) radionuclide therapy for patients with mCRPC (also known as mAPMR, metastatic androgen pathway modulation-resistant prostate cancer).HISTORICAL · Outcome unverifiedPrimary source
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2026-10-19$TLXTelix Pharmaceuticals LimitedEANM 2026, 39th Annual Congress of the European Association of Nuclear Medicine (Vienna), October 19, 2026, 08:00–09:30 CEST: oral presentation (abstract OP-312, presenter Nelleke Tolboom, UMC Utrecht) on IPAX BrIGHT, the pivotal study of TLX101-Tx (iodofalan-131I) with or without lomustine vs lomustine alone in patients with radiographically confirmed recurrent glioblastoma at first recurrence (NCT07100730).HISTORICAL · Outcome unverifiedPrimary source
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2026-10-18$TLXTelix Pharmaceuticals LimitedEANM 2026, 39th Annual Congress of the European Association of Nuclear Medicine (Vienna), October 18, 2026, 15:00–16:30 CEST: oral presentation (abstract OP-170, presenter Ghoufrane Tlili, CHU Bordeaux) on LUTEON, the Phase 3 study to assess safety and efficacy of TLX250-Tx (177Lu-girentuximab) in advanced, relapsed or recurrent clear cell renal cell carcinoma (ccRCC) (NCT07197580).HISTORICAL · Outcome unverifiedPrimary source
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2026-10-19$MANEVERADERMICS INCPart A of Phase 3 Study '304' (536 men with mild-to-moderate pattern hair loss, VDPHL01 8.5 mg once or twice daily vs placebo) met all primary and secondary endpoints. Mean increase in non-vellus target area hair count at Month 6: 28.6 hairs/cm² (once daily) and 36.4 hairs/cm² (twice daily) vs 6.6 with placebo (p<0.0001); 55.7% and 68.7% reported 'improved' or 'much improved' hair coverage vs 15.0% with placebo (p<0.0001). No treatment-related serious adverse events and no adverse events of special interest of cardiac origin. Veradermics anticipates Part B data from Study '302' later in 2026 and Study '306' (women) topline in the first half of 2027. Topline announced October 19, 2026.HISTORICAL · Disclosed eventPrimary source
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2026-10-19$IRONDISC MEDICINE INCAPOLLO Phase 3 (183 adults and adolescents aged 12 or older with EPP or XLP, bitopertin 60 mg once daily vs placebo, 1:1, 6 months) met both co-primary endpoints: whole-blood metal-free PPIX reduction of -41.4% vs placebo (p<0.0001) and +12.2 hours of average monthly total time in light without pain during month 6 vs placebo (p=0.0010). All secondary endpoints were statistically significant, including fewer phototoxic reactions (p<0.0001). Dizziness was the most common adverse event (50%), mild or moderate; no adverse events above Grade 3. Disc plans to resubmit the NDA to the FDA by the end of 2026, with an FDA decision anticipated by mid-2027. Topline announced October 19, 2026.HISTORICAL · Disclosed eventPrimary source
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2026$KRYSKRYSTAL BIOTECH INCInterim data: KB707 · Gorlin syndrome (Phase 1/2). Company timing: 2026. Exact event day is not announced.HISTORICAL · Superseded estimateSEC filing
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2026-10-16$OMEROmeros CorporationThe EMA's CHMP maintained its negative opinion on the marketing authorization application for narsoplimab in transplant-associated thrombotic microangiopathy (TA-TMA) following re-examination, announced October 16, 2026. According to Omeros, an eight-member ad hoc expert group (AHEG) consisting of hematologists, statisticians, and transplant physicians, together with two patient representatives, was convened by the CHMP to address a single, three-part question posed by the CHMP, and recommended a review of individual patient-level data by external experts; Omeros states it submitted detailed patient-level data in August 2026 but that the CHMP did not provide it to the AHEG. Omeros said it does not expect routine access in Europe and is working toward reimbursed named-patient access where permitted, and separately notified the CHMP of its intent to close the compassionate-use program for the drug (U.S. brand name YARTEMLEA) due to rising commercial-supply demand in the United States; patients already on therapy are to receive enough drug to complete their courses.HISTORICAL · Disclosed eventPrimary source
2026-10-16$IBRXIMMUNITYBIO, INC.ImmunityBio reported long-term Phase 2/3 QUILT-3.032 data for ANKTIVA (nogapendekin alfa inbakicept-pmln) plus BCG in BCG-unresponsive NMIBC with CIS, with or without papillary tumors: 84% cystectomy-free survival at 36 months among responders, 71% overall complete response rate, median complete-response duration 26.6 months with responses extending beyond 53 months; published in the Journal of Urology, announced October 16, 2026. This is a long-term follow-up analysis, distinct from the FDA's October 2026 approval of the expanded papillary-only indication already in this catalog.HISTORICAL · Disclosed eventPrimary source
2026-10-15$LEGNLegend Biotech CorporationThe FDA cleared Legend Biotech's IND application for LB2501, an investigational in vivo CD19/CD20 CAR-T therapy built on the TaVec lentiviral platform and being evaluated without lymphodepleting chemotherapy, for relapsed or refractory B-cell malignancies including B-cell non-Hodgkin lymphoma, announced October 15, 2026. A planned US Phase 1/2 study will evaluate safety, tolerability, pharmacokinetics and preliminary efficacy; no start date disclosed. This is distinct from the ongoing Phase 1 study of the same product in China (NCT07002112) already tracked in this catalog.HISTORICAL · Disclosed eventPrimary source
2026-10-15$KRYSKRYSTAL BIOTECH INCKrystal Biotech reported positive proof-of-concept data for KB113 (low-dose intratumoral KB707, delivering IL-2/IL-12) in three adult patients with Gorlin syndrome basal cell carcinomas, announced October 15, 2026: 83.1% of assessed lesions showed clinical regression (69 of 83), with biopsied lesions showing histologically confirmed complete response. The company has begun FDA discussions on advancing KB113's clinical development.HISTORICAL · Disclosed eventPrimary source
2026-10-13$BEAMBEAM THERAPEUTICS INCBeam Therapeutics announced initial Phase 1/2 data for BEAM-301 in glycogen storage disease type Ia (GSDIa): as of the June 26, 2026 data cutoff, six patients had received a single intravenous infusion of BEAM-301 (three at 20 mg, three at 40 mg); median follow-up was 313 days (range, 249–453) in the 20 mg cohort and 53 days (range, 5–110) in the 40 mg cohort, and one patient in the 40 mg cohort was not evaluable for efficacy as of the cutoff. Safety: all patients experienced at least one treatment-emergent adverse event considered related to BEAM-301; five serious adverse events were reported and resolved within two to 10 days, including three Grade 3 infusion-related reactions; all transaminase elevations were transient and resolved without intervention and, except for a single Grade 2 AST elevation, were Grade 1; no dose-limiting toxicities, treatment discontinuations due to treatment-emergent adverse events, or deaths were reported. Efficacy: median time to fasting hypoglycemia at baseline was 2.9 hours in the 20 mg cohort and 2.5 hours in the 40 mg cohort; by Day 36 it increased to 4.3 hours in the 20 mg cohort, while both evaluable patients in the 40 mg cohort achieved the protocol-defined maximum controlled fasting duration of ≥15 hours. Decreases from baseline in prescribed daily starch intake were 74% (Day 128), 71% (Day 227) and 11% (Day 387) in the 20 mg cohort and 71% (Day 50) and 92% (Day 93) in the 40 mg cohort; triglyceride levels were comparable to baseline at last follow-up. The data will be presented as a poster at the ESGCT 33rd Annual Congress on October 28, 2026.HISTORICAL · Disclosed eventPrimary source
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2026-10-13$RYTMRHYTHM PHARMACEUTICALS, INC.Rhythm Pharmaceuticals announced the commercial launch of IMCIVREE (setmelanotide) in Japan for patients with acquired hypothalamic obesity, following the drug's inclusion on Japan's National Health Insurance drug price list; the company says IMCIVREE is the first approved therapy in Japan for this indication. Japan's Ministry of Health, Labour and Welfare approved IMCIVREE for acquired hypothalamic obesity in August 2026, based on the Phase 3 TRANSCEND trial (142 patients, including a Japanese cohort), which met its primary endpoint with an 18.8% placebo-adjusted reduction in BMI; setmelanotide also holds MHLW orphan drug designation for this indication. Rhythm estimates approximately 5,000 to 8,000 people live with acquired HO in Japan.HISTORICAL · Disclosed eventPrimary source
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2026-10-18$GSKGSK plcGSK announced the first global data for risvutatug rezetecan (Ris-Rez), its investigational B7-H3-targeted antibody-drug conjugate, in relapsed extensive-stage small cell lung cancer, from the Phase Ib dose-optimisation portion of EMBOLD PanTumour-101 (NCT06551142), announced October 18, 2026. Confirmed objective response rate was 61% at 8 mg/kg (11/18 evaluable patients; 95% CI: 35.7-82.7) and 32% at 6 mg/kg (7/22; 95% CI: 13.9-54.9); grade 3 or higher treatment-related adverse events occurred in 42% of patients at 8 mg/kg and 15% at 6 mg/kg, mostly haematological; interstitial lung disease occurred in 1 of 50 patients (grade 2). Median follow-up was 100.5 days. The findings will be presented in a poster session at the ESMO Congress 2026 in Madrid. The 8 mg/kg dose is being evaluated in the global Phase III EMBOLD SCLC-301 study.HISTORICAL · Disclosed eventPrimary source
2026-10-18$SYRESpyre Therapeutics, Inc.UEGW 2026 (Barcelona) oral presentation on Sunday, October 18, 15:30-15:40 CEST (Hot Topics in IBD, Room B3, presenter Silvio Danese): efficacy and safety of the half-life extended antibodies SPY001 (anti-α4β7), SPY002 (anti-TL1A) and SPY003 (anti-IL-23) for induction treatment of moderately to severely active ulcerative colitis, the company's first scientific congress presentation of clinical data across all three IBD antibodies. The company release does not report efficacy figures; the SKYLINE combination results are a separate, later milestone.HISTORICAL · Disclosed eventPrimary source
2026-10-15$LLYEli Lilly and CompanyOn October 15, 2026, the EMA's Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending marketing authorisation for Foundayo (orforglipron), a GLP-1 receptor agonist, applicant Eli Lilly Nederland B.V. Indications: as an adjunct to healthy diet and physical activity for weight management, including weight loss and weight maintenance, in adults with an initial BMI of ≥ 30 kg/m2 (obesity), or ≥ 27 kg/m2 to < 30 kg/m2 (overweight) with at least one weight-related comorbidity; and for adults with insufficiently controlled type 2 diabetes, as monotherapy when metformin is considered inappropriate or in combination with other diabetes medicines. Film-coated tablets of 0.8 mg, 2.5 mg, 5.5 mg, 9 mg, 14.5 mg and 17.2 mg. The final decision rests with the European Commission; no timeline disclosed.HISTORICAL · Disclosed eventPrimary source
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2026-10-15$JSPRJasper Therapeutics, Inc.Jasper Therapeutics completed enrollment of the IgA nephropathy (IgAN) cohort of its Phase 2 renal basket study evaluating vensobafusp alfa (KP104), announced October 15, 2026 via Form 8-K. The filing discloses the enrollment milestone only; it does not give a specific date for the next data readout.HISTORICAL · Disclosed eventSEC filing
2026-10-16$VTRSViatris Inc.FDA approved RYZUMVI (phentolamine ophthalmic solution 0.75%) for presbyopia in adults, announced October 16, 2026. The decision is based on the Phase 3 VEGA-2 and VEGA-3 trials, which met the primary endpoint and all key secondary endpoints with no serious treatment-related adverse events; the most common adverse reactions in the presbyopia trials were conjunctival hyperemia (21%) and instillation-site irritation (16%). RYZUMVI was already approved for pharmacologically induced mydriasis in adults and in pediatric patients 3 years of age and older. Opus Genetics (IRD) and Viatris (VTRS) share a global license agreement for the product; Viatris holds exclusive U.S. commercialization rights, and the approval triggers a milestone payment to Opus Genetics. Sources: https://investor.viatris.com/news-releases/news-release-details/viatris-receives-us-fda-approval-ryzumvir-treatment-presbyopia ; https://www.globenewswire.com/news-release/2026/10/16/3382714/0/en/opus-genetics-announces-fda-approval-of-phentolamine-ophthalmic-solution-0-75-for-the-treatment-of-presbyopia.htmlHISTORICAL · Disclosed eventPrimary source
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15–16 October 2026$TSHATAYSHA GENE THERAPIES INCTSHA-102 REVEAL Part A Phase 1/2 safety and efficacy results in Rett syndrome: encore oral and poster presentations on October 15 at the Child Neurology Society meeting. Company-hosted symposium on October 16. These sessions repeat previously shared IRSF data rather than announce a new readout. Company timing: 15–16 October 2026.HISTORICAL · Outcome unverifiedPrimary source
2026-10-16$RHHBYRocheFDA approved Enspryng (satralizumab) for thyroid eye disease (TED) in adults, announced October 16, 2026, as the first and only at-home subcutaneous treatment option for TED; the subcutaneous formulation can be self-administered or given by a caregiver after training by a healthcare provider. The approval followed Priority Review based on the Phase III SatraGO program (258 patients, 19 countries, 1:1 randomization against placebo): in the active-TED population, SatraGO-2 met its primary endpoint (proptosis response 52.9% with Enspryng vs 23.4% with placebo; diplopia response 60.7% vs 25.8%), while SatraGO-1 did not reach statistical significance on the prespecified primary endpoint at week 24. No new safety signals were identified; the safety profile was consistent with the drug's known profile in its first approved indication, neuromyelitis optica spectrum disorder (NMOSD, approved 2020).HISTORICAL · Disclosed eventPrimary source
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2026-10-16$REGNRegeneron Pharmaceuticals, Inc.The EMA's CHMP adopted a positive opinion recommending EU approval of an updated Libtayo (cemiplimab) dosing regimen across all approved cancer indications, announced October 16, 2026. After an initial 12-week cycle of 350 mg every three weeks (30-minute IV infusion), the recommended regimen is 700 mg every six weeks, also as a 30-minute infusion; a shorter 15-30 minute infusion option is also proposed for the 350 mg every-three-weeks dose once the first infusion has been well tolerated at 30 minutes. The 700 mg every-six-week regimen is already approved in the EU, but only for adjuvant treatment of high-risk cutaneous squamous cell carcinoma (CSCC) after surgery and radiotherapy. This is a CHMP recommendation, not a final decision; European Commission approval is expected in the coming months.HISTORICAL · Disclosed eventPrimary source
2026-10-16$IONSIONIS PHARMACEUTICALS INCThe EMA's CHMP adopted a positive opinion recommending EU approval of TRYNGOLZA (olezarsen) for adults with severe hypertriglyceridemia (sHTG, fasting triglycerides at or above 880 mg/dL), as an adjunct to diet and in combination with other lipid-lowering therapies, announced October 16, 2026. This is a CHMP recommendation, not a final decision; European Commission approval is expected in the fourth quarter of 2026. Ionis discovered and developed olezarsen and commercializes it in the United States; Sobi holds exclusive ex-U.S. commercialization rights (excluding Canada and China) under a license agreement with Ionis. The companies cite data from the Phase 3 CORE and CORE2 studies showing triglyceride reductions of up to 72% at six months and an 85% reduction in acute pancreatitis events versus placebo in the pooled analysis.HISTORICAL · Disclosed eventPrimary source
2026-10-16$ASNDAscendis Pharma A/SThe EMA's CHMP adopted a positive opinion recommending EU marketing authorization for a once-weekly TransCon CNP (navepegritide) regimen for the treatment of achondroplasia in children, announced October 16, 2026. This is a CHMP recommendation, not a final decision; approval by the European Commission is a separate, later step.HISTORICAL · Disclosed eventSEC filing
2026-10-15$RVMDRevolution Medicines, Inc.The EMA's Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion recommending EU marketing authorization for RASONQUE (daraxonrasib), a once-daily oral RAS(ON) inhibitor, as monotherapy for adults with metastatic pancreatic adenocarcinoma who received at least one prior systemic therapy. Based on Phase 3 RASolute 302 (overall survival HR 0.40, median 13.2 vs 6.7 months; PFS HR 0.49, median 7.2 vs 3.6 months). Final authorization decision rests with the European Commission; no timeline disclosed. Follows the August 26, 2026 FDA approval.HISTORICAL · Disclosed eventPrimary source
2026-10-14$OPKOPKO Health, Inc.OPKO Health and subsidiary BioReference Health entered a definitive Asset Purchase Agreement, signed October 14, 2026, to sell select clinical and anatomic pathology laboratory testing assets (including women's health, urology, correctional-services testing and the proprietary 4Kscore prostate-cancer test) to Laboratory Corporation of America Holdings (Labcorp). Consideration: $722 million cash upfront at closing (subject to revenue-based adjustments) plus up to $150 million in earnouts over up to ten years tied to 4Kscore sales. Closing is subject to HSR Act clearance and customary conditions, with an outside date of April 14, 2027; the deal is not subject to a financing condition.HISTORICAL · Disclosed eventSEC filing
End of November 2026$MLTXMoonLake ImmunotherapeuticsSonelokimab HS BLA acceptance, Priority Review decision and PDUFA date allocation. Superseded by the BLA submission of September 30, 2026: the company said it expects to learn whether the BLA is accepted for review within about 60 days of submission and to receive the planned review timeline within about 74 days. As of October 15, 2026, MoonLake had not announced FDA acceptance of the BLA or a PDUFA date. |HISTORICAL · Superseded estimatePrimary source
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2026-10-14$IBRXIMMUNITYBIO, INC.FDA approved the expanded indication for ANKTIVA (nogapendekin alfa inbakicept-pmln) in combination with BCG, announced October 14, 2026, ahead of the January 6, 2027 target action date. The label now reads: indicated for the treatment of adult patients with BCG-unresponsive non-muscle invasive bladder cancer, adding papillary-only tumors to carcinoma in situ with or without papillary tumors.HISTORICAL · Disclosed eventSEC filing
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2026-10-14$TRDATRDAEntrada reported ELEVATE-45-201 Cohort 1 results for ENTR-601-45 (5 mg/kg, three doses, eight participants randomized 3:1): favorable safety and tolerability; dystrophin +0.10 percentage points from baseline in treated participants versus -0.02 on placebo, exon skipping +0.15 versus -0.04. Cohort 2 (10 mg/kg) data are guided to H1 2027.HISTORICAL · Disclosed eventPrimary source
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2026-10-13$UTHRUNITED THERAPEUTICS CORPORATIONUnited Therapeutics and Liquidia announced a global settlement resolving all pending patent, trade-secret and antitrust litigation between them over Liquidia's YUTREPIA and Treprostinil Injection. The settlement follows the September 30, 2026 ruling that claims 1 and 14 of United Therapeutics' U.S. Patent No. 11,826,327 are valid and infringed; Liquidia will not appeal and will pay United Therapeutics a net $175 million within 30 business days, plus two $72.7 million installments due January 31 and April 30, 2027 (total net payments of $380.7 million through 2026-2027, including $60.3 million paid in October 2026 to other antitrust-case parties). Liquidia is removing the PH-ILD indication from YUTREPIA's label and has ended its Treprostinil Injection promotional agreement; United Therapeutics retains the ability to assert its patents against Liquidia's other development programs or future products.HISTORICAL · Disclosed eventPrimary source
October 13, 2026$STROSutro Biopharma, Inc.World ADC plenary on the early clinical safety and pharmacokinetic profile of STRO-004, October 13 at 9:30 a.m. Pacific Time. Separate STRO-006 and STRO-227 presentations concern preclinical findings.HISTORICAL · Outcome unverifiedPrimary source
2026-10-13$LQDALIQUIDIA CORPLiquidia and United Therapeutics announced a global settlement resolving all pending patent, trade-secret and antitrust litigation between them. Liquidia will not appeal the September 30, 2026 ruling that claims 1 and 14 of U.S. Patent No. 11,826,327 are valid and infringed, and will pay United Therapeutics a net $175 million within 30 business days, plus two $72.7 million installments due January 31 and April 30, 2027; a separate $60.3 million was paid in October 2026 to other parties in the related antitrust litigation, for net payments of $380.7 million through 2026-2027. YUTREPIA remains available without disruption for pulmonary arterial hypertension; Liquidia is removing the PH-ILD indication from YUTREPIA's label, has stopped promoting it for PH-ILD, and has ended its Treprostinil Injection promotional agreement. United Therapeutics retains the ability to assert its patents against Liquidia's other development programs or future products.HISTORICAL · Disclosed eventPrimary source
ECNP Congress 2026-10-10–2026-10-13$GHRSGH RESEARCH PLCConference presentation: mebufotenin (GH001) · TRD Treatment-resistant depression (Phase 2b). Company timing: ECNP Congress 2026-10-10–2026-10-13. Congress: ECNP Congress. The conference range does not establish the individual presentation day.HISTORICAL · Outcome unverifiedSEC filing
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2026-10-13$GENBGENERATE BIOMEDICINES INCGenerate Biomedicines and Zealand Pharma announced a collaboration and license agreement to develop AI-engineered multispecific protein therapeutics for obesity and other metabolic and cardiometabolic diseases, covering two initial programs with an option to add a third. Generate will lead research through lead-candidate selection using its generative AI platform; Zealand Pharma will lead clinical development, regulatory submissions and worldwide commercialization. Generate will receive a $30 million upfront payment, up to $35 million in early preclinical milestones, total milestones of nearly $1.2 billion across the programs, and tiered royalties on worldwide net sales of any resulting products.HISTORICAL · Disclosed eventPrimary source
2026-10-13$BMEABiomea Fusion, Inc.Biomea Fusion reported Phase 1 results (study GLP-131, NCT07223216) for BMF-650, its investigational oral GLP-1 receptor agonist: mean weight reduction of 1.5%-3.2% by Day 29 across four multiple-ascending-dose cohorts versus 0.1% for pooled placebo, about 0.97 kg per week at once-daily doses of 200 mg or higher. A separate, confined fifth cohort (200 mg for one week, then 400 mg) showed a 6.1% (6.2 kg) mean reduction, about 1.55 kg per week; the company says this cohort should be read separately because confinement altered the placebo group's eating. All treatment-emergent adverse events across the 40 active-dose participants were mild or moderate, with no severe or serious TEAEs, dose modifications or discontinuations. The company plans to complete longer-term toxicology studies and pursue a strategic partnership before further clinical development; its primary pipeline focus remains icovamenib in diabetes.HISTORICAL · Disclosed eventPrimary source
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2026-10-13$ALECAlector, Inc.Alector virtual R&D event October 13 at 8 a.m. PT covering ABC-enabled AL137, AL164, AL062 and ADP065. Preclinical pipeline discussion; no human efficacy readout is claimed.HISTORICAL · Outcome unverifiedPrimary source
2026-10-12$SNDXSyndax Pharmaceuticals, Inc.MAXPIRe Phase 2 (145 patients with idiopathic pulmonary fibrosis, axatilimab 0.3 mg/kg every two weeks vs placebo, 2:1) did not meet its primary endpoint, the annualized rate of decline in forced vital capacity. Safety was comparable to placebo with no new signals. Syndax does not plan further development of axatilimab in IPF; cGVHD trials continue. Topline announced October 12, 2026 after market close.HISTORICAL · Disclosed eventPrimary source
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2026-10-12$REGNRegeneron Pharmaceuticals, Inc.Regeneron reported positive 84-week Phase 3 OPTIMA results for Pasatru (garetosmab-grts) in adults with fibrodysplasia ossificans progressiva at ASBMR: zero new heterotopic ossification lesions during the trial extension and sustained reduction in flare-ups, with a consistent safety profile from week 56 to 84.HISTORICAL · Disclosed eventPrimary source
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2026-10-12$NRIXNurix Therapeutics, Inc.In its fiscal third-quarter update, Nurix discontinued further clinical development of NX-2127 (zelebrudomide) as part of a strategic prioritization of its wholly owned oncology portfolio; it also reported the first patient enrolled in the Phase 3 DAYBreak CLL-306 trial of bexobrutideg versus pirtobrutinib.HISTORICAL · Disclosed eventPrimary source
2026-10-12$JNJJohnson & JohnsonJohnson & Johnson announced TREMFYA Crohn's disease data being presented as posters at ACG 2026 on October 13: in the GALAXI 2 and 3 Week 144 long-term extension (as-observed analysis), clinical remission was 94% (100 mg q8w) and 91% (200 mg q4w) and endoscopic remission 52% and 61%; prespecified FUZION subgroup analyses in perianal fistula were consistent with the overall Week 24 combined fistula remission results (28% and 27% vs 10% with placebo).HISTORICAL · Disclosed eventPrimary source
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2026-10-12$EWTXEdgewise Therapeutics, Inc.Phase 1 healthy-adult data for EDG-15400 were scheduled for presentation at HFSA on October 12, 2026 (12:15–1:15 p.m. Mountain Time). These are not Phase 2 HFpEF efficacy results.HISTORICAL · Outcome unverifiedPrimary source
October 12, 2026$EPRXEupraxia Pharmaceuticals Inc.ACG poster on EP-104GI in the RESOLVE Phase 1b/2 trial, dysphagia improvements through 52 weeks, scheduled for October 12, 2026. The related UEG dysphagia poster on October 18 is a repeat presentation, not a second clinical readout.HISTORICAL · Outcome unverifiedPrimary source
2026-10-12$CYTKCYTOKINETICS INCAdditional ACACIA-HCM analyses in non-obstructive HCM presented at HFSA 2026: at 36 weeks aficamten significantly improved the composite exercise score BEAP-RS versus placebo (p<0.001). Cytokinetics plans to submit a supplemental NDA this quarter.HISTORICAL · Disclosed eventPrimary source
2026-10-12$CSTLCastle Biosciences, Inc.Castle Biosciences announced data from three TissueCypher Barrett's esophagus studies (two case reports and one multicenter study) on molecular risk information beyond histopathology, presented as posters at ACG 2026 on October 12 and 13. Diagnostic-test data, not a drug trial.HISTORICAL · Disclosed eventPrimary source
2026-10-12$AVBPARRIVENT BIOPHARMA INCArriVent dosed the first U.S. patient in the Phase 1 trial of ARR-002 (NCT07755436), a MUC16/NaPi2b dual-target tetravalent antibody-drug conjugate for ovarian and endometrial cancer. The company has not disclosed timing for initial data.HISTORICAL · Disclosed eventPrimary source
October 12 announcement$ZBIOZenas BioPharma, Inc.Zenas announced new INDIGO Phase 3 extension and steroid-toxicity analyses in IgG4-related disease, presented at the October 8–10 symposium. Vaccine-response observations came from a small exploratory substudy, not a separate pivotal trial.HISTORICAL · Disclosed eventCompany release
2026-10-12$TRAXFIRST TRACKS BIOTHERAPEUTICS INCANB033 Phase 1b celiac-disease Cohort 1 gluten-challenge results showed statistically significant protection against intestinal damage and symptoms versus placebo. The placebo-adjusted villus-height/crypt-depth change was +0.49 (p=0.009). These are early-stage results in 32 patients, distinct from the pending mucosal-healing Cohort 2.HISTORICAL · Disclosed eventCompany release
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October 12 announcement$TGTXTG Therapeutics, Inc.TG announced publication of a five-year matching-adjusted indirect comparison of BRIUMVI with ocrelizumab and ofatumumab in relapsing MS. Reported favorable associations are not evidence from a randomized head-to-head comparison.HISTORICAL · Disclosed eventCompany release
October 12 announcement$STOKStoke Therapeutics, Inc.Stoke disclosed ADOA natural-history and preclinical STK-002 findings at AAO. These support the ongoing OSPREY program; the separate initial safety and efficacy readout from cohorts 3 and 4 remains expected in H1 2027.HISTORICAL · Disclosed eventCompany release
October 12 announcement$PVLAPALVELLA THERAPEUTICS INCPalvella disclosed new SELVA Phase 3 participant-interview and maximal-use pharmacokinetic analyses at Fall Clinical, alongside separate DSAP claims research. These are additional analyses, not a new pivotal efficacy readout.HISTORICAL · Disclosed eventCompany release
October 12 announcement$PALIPalisade Bio, Inc.ACG disclosure of clinical, PK/PD and mechanistic findings from small, short, open-label ulcerative-colitis and fibrostenotic Crohn’s cohorts. The findings support Phase 2 investigation but do not establish efficacy in controlled trials.HISTORICAL · Disclosed eventCompany release
October 12 announcement$NGENNervGenNervGen announced the first participant dosed in RESTORE, a Phase 3 registrational study in chronic cervical motor-incomplete spinal cord injury. October 12 is the announcement date.HISTORICAL · Disclosed eventCompany release
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2026-10-12$MIRMMirum Pharmaceuticals, Inc.LIVMARLI EXPAND Phase 3 met its primary pruritus endpoint and all five prespecified secondary endpoints in ultra-rare cholestatic liver diseases. In the pediatric primary analysis, the placebo-adjusted pruritus improvement was 0.98 points (p=0.0004). Results announced October 12, 2026.HISTORICAL · Disclosed eventPrimary source
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October 12 announcement$CRVOCervoMed Inc.CervoMed announced initial 12-week open-label nfvPPA biomarker findings presented at ISFTD. Mean plasma NfL declined; GFAP was stable. Biomarker changes in this small uncontrolled period do not establish clinical benefit.HISTORICAL · Disclosed eventPrimary source
2026-10-12$BMYBRISTOL MYERS SQUIBBThe planned ACTION-1 Phase 3 interim analysis met the progression-free-survival primary endpoint in SSTR-positive GEP-NETs progressing after Lu177-based therapy. Overall-survival follow-up continues; detailed results will be presented at a future medical meeting with no date specified.HISTORICAL · Disclosed eventPrimary source
2026-10-12$BMYBRISTOL MYERS SQUIBBALOFT-IPF Phase 3 met its Week 52 forced-vital-capacity primary endpoint with admilparant 60 mg twice daily versus placebo. The 120 mg twice-daily arm was not statistically significant. Regulatory discussions and detailed presentation are planned without a disclosed date.HISTORICAL · Disclosed eventPrimary source
2026-10-11$PHATPhathom Pharmaceuticals, Inc.ACG poster P0624, 3:30–7 p.m. CDT: post-hoc BMI analysis of vonoprazan efficacy in non-erosive GERD. Exploratory analysis, not a new pivotal trial result.HISTORICAL · Outcome unverifiedPrimary source
October 8–11, 2026$LLYEli Lilly and CompanyNew Fall Clinical dermatology findings include Phase 3 ADorable-1 pediatric lebrikizumab data and TOGETHER-PsO analyses. October 8–11 is the conference window; individual poster days are not provided.HISTORICAL · Outcome unverifiedPrimary source
October 11, 2026$BMRNBioMarin Pharmaceutical Inc.ASBMR poster 483, October 11 at 2:00-3:30 p.m. EDT: new post-hoc VOXZOGO imaging analysis of foramen magnum and craniocervical junction growth in children with achondroplasia. Scheduled clinical presentation; no inference of completed presentation from calendar date.HISTORICAL · Outcome unverifiedPrimary source
2026-10-11$BBIOBridgeBio Pharma, Inc.CALIBRATE Phase 3 ASBMR analyses reported increased bone-turnover markers and restoration of endogenous PTH with encaleret in ADH1. These are additional analyses of the trial, not a new pivotal topline.HISTORICAL · Disclosed eventCompany release
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2026-10-11$BBIOBridgeBio Pharma, Inc.CALIBRATE patient-reported ASBMR analyses found improvement in at least one ADH1 symptom in 100% of encaleret participants versus 46% on standard care. The analysis is distinct from the bone-turnover presentation.HISTORICAL · Disclosed eventCompany release
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2026-10-11$BBIOBridgeBio Pharma, Inc.Independent Epic COSMOS observational ATTR-CM analysis presented at HFSA found acoramidis associated with lower risk of the composite clinical endpoint than tafamidis. This is real-world comparative evidence, not a randomized head-to-head trial.HISTORICAL · Disclosed eventCompany release
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October 11 announcement$BBIOBridgeBio Pharma, Inc.BridgeBio announced the first participant dosed in RECLAIM-HP Phase 3 in chronic hypoparathyroidism. This program is separate from the ADH1 CALIBRATE trial and the existing May 8, 2027 ADH1 PDUFA target.HISTORICAL · Disclosed eventCompany release
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8–11 October 2026$ATTOATTOVIA THERAPEUTICS INCATTO-1310 Phase 1b interim efficacy and safety poster in atopic dermatitis or chronic pruritus at Fall Clinical Dermatology Conference. The EADV posters concern separate healthy-volunteer and translational datasets. Company timing: 8–11 October 2026. Congress: Fall Clinical Dermatology Conference 2026. The conference range does not establish the individual presentation day.HISTORICAL · Outcome unverifiedPrimary source
8–11 October 2026$ATTOATTOVIA THERAPEUTICS INCPreclinical characterization of ATTO-2306, a long-acting bispecific antibody targeting IL-13 and IL-31, presented at Fall Clinical Dermatology Conference. Company timing: 8–11 October 2026. Congress: Fall Clinical Dermatology Conference 2026. The conference range does not establish the individual presentation day.HISTORICAL · Outcome unverifiedPrimary source
2026-10-10$BBIOBridgeBio Pharma, Inc.ATTRibute-CM sub-analyses presented at HFSA assessed cardiovascular hospitalization burden and mortality. The October 11 release confirms presentation; the previously scheduled session was October 10.HISTORICAL · Disclosed eventCompany release
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2026-10-09$ANIPANI PHARMACEUTICALS INCSYNCHRONICITY Phase 4 open-label, single-arm data were presented at AAO on October 9 and announced October 12. Both six-month co-primary endpoints were met; functional and anatomic improvements were generally maintained at 24 months. There was no randomized comparator.HISTORICAL · Disclosed eventCompany release
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August 2026$PVLAPALVELLA THERAPEUTICS INCPalvella completed the rolling NDA submission for QTORIN rapamycin in microcystic lymphatic malformations in August 2026, as stated in its October 12 release. The source specifies the month, not the completion day.HISTORICAL · Disclosed eventCompany release
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2025-11-21$PFEPfizer Inc.FDA approved perioperative Padcev with Keytruda or Keytruda Qlex for adults with muscle-invasive bladder cancer ineligible for cisplatin on November 21, 2025, ahead of the former April 7, 2026 target. This is the KEYNOTE-905/EV-303 indication.HISTORICAL · Disclosed eventPrimary source
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2025-11-21$MRKMerck & Co., Inc.FDA approved perioperative Padcev with Keytruda or Keytruda Qlex for adults with muscle-invasive bladder cancer ineligible for cisplatin on November 21, 2025, ahead of the former April 7, 2026 target. This is the KEYNOTE-905/EV-303 indication.HISTORICAL · Disclosed eventPrimary source
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2026-10-10 announcement$RHHBYF. Hoffmann-La Roche LtdRoche announced 52-week MEERKAT/SANDCAT data in uveitic macular edema and FDA acceptance of the vamikibart BLA. The AAO presentation is distinct from the primary 16-week analyses presented in 2025.HISTORICAL · Disclosed eventPrimary source
October 10, 2026$MRKMerck & Co., Inc.One-year BRUNELLO Phase 2b/3 results for remigromig in diabetic macular edema presented at AAO October 10. Both doses met visual-acuity non-inferiority versus ranibizumab; no secondary endpoint showed superiority. Proliferative diabetic retinopathy adverse events and discontinuations were more frequent with remigromig. Not an approval.HISTORICAL · Disclosed eventPrimary source
2026-10-10$KODKodiak Sciences Inc.AAO presentation of GLOW2 Phase 3 results in diabetic retinopathy, October 10 at 4:51 p.m. CT.HISTORICAL · Outcome unverifiedPrimary source
October 9, 2026$VRTXVertex Pharmaceuticals IncorporatedVertex announced NACFC interim ALYFTREK open-label extension data in children aged 2-5 with cystic fibrosis, including recovery of exocrine pancreatic function in some children and pancreatic-enzyme replacement discontinuation. October 9 is the release date; no exact poster date is asserted. Not an approval for this age group.HISTORICAL · Disclosed eventPrimary source
October 9, 2026$TEVATeva Pharmaceutical Industries Ltd.Teva announced FDA approval of WELTRUZA (olanzapine; TEV-749), a once-monthly subcutaneous long-acting injection for adults with schizophrenia. October 9 is the announcement date; the former Q4 2026 estimated decision is no longer pending.HISTORICAL · Disclosed eventPrimary source
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October 9, 2026$MNKDMannKind CorporationMannKind disclosed new Furoscix ReadyFlow PK/PD and cross-study analyses ahead of HFSA presentations, supporting comparable diuretic responses to IV furosemide and the on-body infusor. October 9 at 20:00 ET is the news-release date (URL uses UTC October 10). Analyses of an approved product, not a new FDA approval or a pivotal efficacy readout.HISTORICAL · Disclosed eventPrimary source
October 9, 2026$MLYSMineralys Therapeutics, Inc.October 9 AHA Hypertension release: new Launch-HTN analysis and final Explore-OSA results. Lorundrostat reduced morning blood pressure in Explore-OSA, with no measurable change in apnea-hypopnea indices. Separate from November AHA Transform-HTN extension and October ASN CKD presentations; do not mark those completed.HISTORICAL · Disclosed eventPrimary source
2026-10-09$KODKodiak Sciences Inc.Official AAO DAYBREAK presentation materials are publicly available. The presentation was scheduled for October 9. The September 28 topline remains a separate historical event.HISTORICAL · Disclosed eventPrimary source
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2026-10-09$KODKodiak Sciences Inc.Official presentation materials for the APEX Phase 1b KSI-101 presentation at AAO, scheduled October 9, are publicly available. Separate from the pending PEAK Phase 3 readout in December 2026.HISTORICAL · Disclosed eventPrimary source
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October 9, 2026$JNJJohnson & JohnsonJ&J announced ICONIC-LEAD icotrokinra Week 112 results in plaque psoriasis presented at Fall Clinical: sustained skin clearance and no new safety signals reported. October 9 is the announcement date; this is long-term clinical data, not a new approval.HISTORICAL · Disclosed eventPrimary source
October 9, 2026$GKOSGlaukos CorporationGLK-101-04 Phase 4 iDose TR with cataract surgery met the primary endpoint versus cataract surgery alone in open-angle glaucoma or ocular hypertension. Month-3 mean IOP reduction was 11.1 versus 7.4 mmHg; reported treatment effect 3.6 mmHg (p<0.0001). This is clinical topline, not a new regulatory approval.HISTORICAL · Disclosed eventPrimary source
October 9, 2026$BMRNBioMarin Pharmaceutical Inc.BioMarin disclosed that it recently submitted a VOXZOGO (vosoritide) sNDA for hypochondroplasia. October 9 is the disclosure date, not the actual filing day. No hypochondroplasia FDA action date is supplied; distinct from the existing February 28, 2027 achondroplasia full-approval PDUFA.HISTORICAL · Disclosed eventPrimary source
October 9, 2026$ALMSAlumis Inc.October 9 Fall Clinical release: new ONWARD1/2 and ONWARD3 envudeucitinib analyses of scalp disease, itch and quality of life in plaque psoriasis, including sustained long-term responses. Additional analyses, not a new primary-endpoint topline or approval.HISTORICAL · Disclosed eventPrimary source
2026-10-08 approval; announced October 9$RHHBYRocheFDA approved Tecentriq plus a fluoropyrimidine and oxaliplatin on October 8, 2026 for adjuvant treatment of stage III dMMR colon cancer in adults and children aged two years or older. Tecentriq Hybreza combination was approved for patients aged 12 or older weighing at least 40 kg. Roche announced the decision October 9.HISTORICAL · Disclosed eventPrimary source
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October 8, 2026$PHVSPharvaris N.V.RAPIDe-3 deucrictibant immediate-release on-demand HAE results published in The Lancet, announced October 8. Primary and 11 secondary endpoints met; this is publication of results, not a new topline event. Distinct from CHAPTER-3 XR prophylaxis and the pending April 23, 2027 IR PDUFA.HISTORICAL · Disclosed eventPrimary source
October 7, 2026$RHHBYRoche Holding AGPartner Zealand announced ZUPREME-2 topline in 220 participants with overweight/obesity and type 2 diabetes: primary endpoint met, with up to 9.2% mean weight loss at week 28 versus 2.0% placebo under the efficacy estimand. Original release October 7; October 8 news coverage is not a second event.HISTORICAL · Disclosed eventPrimary source
2026-10-08$BBIOBridgeBio PharmaCommercial Day in New York City: commercial readiness and launch strategy across three planned launches. Corporate event, not an FDA decision. Time not specified in the source.HISTORICAL · Outcome unverifiedPrimary source
2026-10-08 announcement$VIRVir Biotechnology, Inc.Vir announced FDA Fast Track for VIR-5500 in late-line metastatic castration-resistant prostate cancer, co-developed with Astellas. Designation is not approval; the exact designation day was not separately disclosed.HISTORICAL · Disclosed eventPrimary source
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2026-10-08 announcement$SRRKScholar Rock Holding CorporationScholar Rock resubmitted the EMA marketing-authorisation application for apitegromab in spinal muscular atrophy with an alternative fill-finish facility. Resubmission is not EU approval.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$PCRXPacira BioSciences, Inc.Viatris agreed to acquire Pacira for $36.50 per share in cash, approximately $1.65 billion equity value. The transaction is announced, not closed; tender of a majority of shares and expiration of the applicable regulatory waiting period remain conditions.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$GKOSGLAUKOS CORPORATIONGlaukos licensed retinal tri-specific biologic RO-104 and rights to discover up to four additional candidates using RevMod. Reported efficacy is preclinical; financial terms and a human-trial start date were not disclosed.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$EWTXEdgewise Therapeutics, Inc.First patient dosed in Phase 2 EQUINOX-HFpEF, targeting approximately 90 participants with HFpEF and left-ventricular ejection fraction of at least 50%. October 8 is the announcement; actual dosing day is undisclosed.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$EDITEditas Medicine, Inc.EDIT-401 Phase 1/2 Strive in HeFH received Australian HREC approval and completed the TGA Clinical Trial Notification process. New Zealand review is pending; this is neither FDA clearance nor confirmation of first dosing.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$CGEMCullinan Therapeutics, Inc.First patient dosed in the planned registrational Phase 2 study of CLN-049 in relapsed/refractory AML. The existing December Phase 1 update remains a separate milestone.HISTORICAL · Disclosed eventPrimary source
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2026-10-08 announcement$CATXPerspective Therapeutics, Inc.Perspective announced FDA Fast Track for PSV359 in adults with locally advanced unresectable and/or metastatic FAP-positive solitary fibrous tumors. This is a development designation, not marketing approval; actual designation day undisclosed.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$BMYBRISTOL MYERS SQUIBBEXCALIBER-RRMM Phase 3 in 800 patients with relapsed/refractory multiple myeloma: reported PFS hazard ratio 0.49 and median PFS 42 versus 20 months. This is a new PFS analysis, not a new FDA approval; detailed results planned at ASH without an individual presentation day in the release.HISTORICAL · Disclosed eventPrimary source
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2026-10-08 announcement$BHVNBiohaven Ltd.Biohaven announced an Ono license for IgG degraders in Japan and selected Asian markets, including Phase 3 Graves’ disease candidate BHV-1300. Upfront $80 million at closing plus a conditional $20 million payment within one year; not $100 million guaranteed upfront.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$ARGXARGENX SEargenx plans to discontinue the Phase 3 UNITY study in Sjögren’s disease following an independent committee futility recommendation. No new safety signal was identified. This does not establish discontinuation of other efgartigimod programs.HISTORICAL · Disclosed eventPrimary source
2026-10-08 announcement$ARGXARGENX SEPositive Phase 2 celiac-disease topline in 126 participants under a controlled gluten challenge. FB102 met the primary villous-height/crypt-depth endpoint at day 78 (p=0.0176). Phase 3 is planned without a disclosed start day; results do not yet establish approval.HISTORICAL · Disclosed eventPrimary source
Trial registry
2026-10-07 announcement$VTVTvTv Therapeutics Inc.vTv announced FDA orphan-drug designation for investigational HPPD in sickle cell disease. Supporting results are preclinical; designation is not approval or proof of efficacy in patients.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$VALNValneva SEValneva reported MHRA revocation of the UK IXCHIQ marketing authorisation after benefit-risk reassessment, without a new safety signal. Licences in other jurisdictions remain unchanged according to the issuer; no appeal is planned.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$RCKTRocket Pharmaceuticals, Inc.Rocket disclosed updated Danon disease findings after its October 6 webinar. The first three patients at the recalibrated dose completed the initial observation period without reported TMA or capillary-leak findings; evidence remains preliminary after serious toxicity at the original dose. The pivotal efficacy population targets 12 males with 12-month co-primary endpoints.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$PFEPfizer Inc.FDA approved tucatinib with trastuzumab and pertuzumab for maintenance treatment of adults with unresectable locally advanced or metastatic HER2-positive breast cancer following induction therapy. Decision October 7; this is an approval, not an upcoming PDUFA.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$NVSNovartis AGNovartis announced FDA approval of Rhapsido for symptomatic dermographism, expanding beyond chronic spontaneous urticaria. The indication is symptomatic dermographism, not all forms of chronic inducible urticaria.HISTORICAL · Disclosed eventPrimary source
October 6–7, 2026$GRALGRAIL, Inc.Six EDCC posters include new NHS-Galleri analyses and PATHFINDER 2 detection performance. The listed posters are scheduled October 6–7; the conference continues through October 8. Scheduled presentation is not proof of completion.HISTORICAL · Outcome unverifiedPrimary source
2026-10-07 announcement$GKOSGLAUKOS CORPORATIONGlaukos reported three-year GLK-202-03 keratoconus extension topline after Epioxa: 38 eyes from 35 subjects, with 92% completing the year-three visit. Follow-up after the pivotal study, not a new FDA approval.HISTORICAL · Disclosed eventPrimary source
October 2 effective; October 8 announcement$AGENAgenus Inc.Armenian conditional marketing authorizations for BOT+BAL became effective October 2, announced October 8, for previously treated adult MSS metastatic colorectal cancer without active liver metastases. Each authorization lasts one year and is renewable; these are not FDA approvals.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$RNXTRenovoRxRenovoRx announced first enrollment in University of Vermont investigator-initiated PRISM-TAMP for borderline resectable pancreatic cancer. The approximately 10-patient study evaluates delivery of gemcitabine with RenovoCath. October 7 is the announcement date; the actual enrollment day is undisclosed. ClinicalTrials.gov still lists NOT_YET_RECRUITING at this check; the issuer announcement is distinguished from the registry status.HISTORICAL · Disclosed eventPrimary source
Trial registry
2026-10-07 announcement$MAIAMAIA Biotechnology, Inc.MAIA announced completion of enrollment in Part C of THIO-101 Phase 2 in NSCLC. This does not mean the entire trial is completed or new final efficacy results are available. Actual completion day undisclosed.HISTORICAL · Disclosed eventPrimary source
Trial registry
2026-10-07 announcement$LPCNLipocine Inc.Lipocine announced Health Canada approval of oral TLANDO testosterone replacement therapy. October 7 is the release date; the regulator’s decision day is not separately stated. This is Canadian authorization, not a new FDA decision.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$ICUSeaStar MedicalSeaStar announced FDA Breakthrough Device Designation for SCD in adult sepsis-related hyperinflammation. This seventh designation is not marketing approval. The announcement gives no exact day for the forthcoming sepsis-subgroup data.HISTORICAL · Disclosed eventPrimary source
2026-10-07 announcement$BLLNBillionToOne, Inc.BillionToOne announced a retrospective liquid-biopsy comparison in advanced solid tumors, published in The Journal of Liquid Biopsy: 169 paired samples from 61 patients. This is diagnostic-monitoring validation, not a randomized therapeutic efficacy trial or FDA approval.HISTORICAL · Disclosed eventPrimary source
Supporting source
2026-10-07 announcement$ARWRArrowhead PharmaceuticalsArrowhead announced FDA STAR pilot entry for the planned plozasiran sHTG supplemental application. This is a review pathway, not approval of the sHTG indication; the entry decision day is not separately disclosed.HISTORICAL · Disclosed eventPrimary source
Supporting source
2026-10-07 announcement$ARVNArvinas, Inc.Arvinas reported final Phase 1 Parkinson’s disease data at MDS: 24 patients treated for 28 days, with exploratory oculomotor and CSF biomarker analyses. The study was not designed to establish clinical efficacy. October 7 marks the release.HISTORICAL · Disclosed eventPrimary source
Supporting source
2026-10-06 announcement$QNTMQuantum BioPharma Ltd.Quantum announced a study start-up agreement with Thermo Fisher Scientific’s clinical research business for planned Phase 2 Lucid-MS in progressive multiple sclerosis. A CRO agreement is not evidence of first patient dosing; no readout day is given.HISTORICAL · Disclosed eventPrimary source
2026-10-06 announcement$JUNSJupiter Neurosciences, Inc.Jupiter announced first dosing in investigator-sponsored Phase 2a RESET in Parkinson’s disease, with approximately 30 patients planned. October 6 is the release date; actual dosing day and future public readout date were not specified.HISTORICAL · Disclosed eventPrimary source
Supporting source
Trial registry
September 30 closing; disclosed October 6$BYSIBeyondSpring Inc.BeyondSpring disclosed October 6 that the sale of BeyondSpring Limited and subsidiaries to Biolin closed September 30. Consideration includes DUBLIN-4 plinabulin data rights outside China, Hong Kong, Macau and Taiwan and trial funding; no public readout date is given.HISTORICAL · Disclosed eventPrimary source
October 7 publication$NRIXNurix Therapeutics, Inc.The Nurix IR release published October 7 at 01:00 ET announced that the first patient had enrolled in Phase 1b/2 NX-5948-203 (NCT07520006), testing bexobrutideg plus venetoclax in CLL/SLL under the Roche collaboration. Its text bears an October 6 dateline. The actual enrollment day was not disclosed; this row marks publication, not a future readout.HISTORICAL · Enrollment announcedPrimary source
October 6 announcement$CRBUCaribou Biosciences, Inc.Caribou announced plans to discontinue further development of vispa-cel and CB-011 while evaluating strategic alternatives. The SEC 8-K says the board approved the plan October 2; October 6 is the public announcement date. Formal termination of individual trials is not inferred.HISTORICAL · Planned discontinuationPrimary source
2026-10-06$VKTXViking TherapeuticsInitiation of the 195-participant, 33-week Part 2 maintenance study announced October 6. Following weekly subcutaneous induction, it evaluates daily/weekly oral and less-frequent subcutaneous maintenance; distinct from Part 1 and VANQUISH.HISTORICAL · Reported outcomePrimary source
2026-10-06$TLXTelix Pharmaceuticals LimitedFirst commercial patients dosed with Pixclara for glioma imaging, announced October 6, marking US commercial availability. FDA approval was earlier; this is not a new approval or trial initiation.HISTORICAL · Reported outcomePrimary source
2026-10-06$SXTP60 Degrees Pharmaceuticals, Inc.October 6 announcement: the October 1 DSMB recommended completing the planned 33-patient hospitalized-babesiosis study. The company elected to stop at 30 enrolled patients for seasonal recruitment reasons. Data remain blinded; no efficacy outcome was released. The scheduled webinar is not assumed completed.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-06$SCYXSCYNEXIS, Inc.Phase 1 results in 25 healthy volunteers reported October 6: safety, tolerability and pharmacokinetic findings; not clinical efficacy evidence.HISTORICAL · Reported outcomePrimary source
2026-10-06$OSTXOS Therapies IncorporatedFinal Phase 2b three-year overall survival in pulmonary metastatic osteosarcoma reported at 72.7%, versus 45.8% in combined historical controls. Nonrandomized comparison, not a concurrent randomized trial.HISTORICAL · Reported outcomePrimary source
2026-10-06$OKYOOKYO Pharma LimitedOKYO announced the first patients enrolled in pivotal Phase 3 NEPTUNE, evaluating urcosimod for neuropathic corneal pain. Actual first-enrollment date was not disclosed.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-06$KAPAKairos PharmaInterim prostate-cancer data reported October 6: median PFS 17.7 versus 2 months, p=0.0008. Interim findings from an evolving protocol are not final confirmatory evidence.HISTORICAL · Reported outcomePrimary source
2026-10-06$HSCSHeartSciences Inc.FDA 510(k) clearance K260005 for the MyoVista wavECG 12-lead resting electrocardiograph announced October 6. Clearance excludes the AI-ECG algorithm; the company gives no commercialization timeline and does not intend to launch without a cleared algorithm.HISTORICAL · Reported outcomePrimary source
2026-10-06$AVBPARRIVENT BIOPHARMA INCFURVENT in first-line EGFR exon 20 insertion NSCLC missed its primary BICR progression-free survival endpoint. The 240 mg arm had median PFS 11.0 versus 9.5 months, HR 0.75, p=0.0654. Secondary signals do not reverse the primary-endpoint miss; overall survival remains immature.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-05$ORICORIC Pharmaceuticals, Inc.Cancer Research UK will fund and sponsor CTA-enabling studies and Phase 1/2 development of ORIC-259, a CIP2A mRNA degrader. ORIC retains an option to reacquire rights after Phase 1/2 data; no trial-start date is announced.HISTORICAL · Reported outcomePrimary source
2026-10-05$KRROKorro Bio, Inc.Korro announced first-cohort dosing of KRRO-121 in healthy volunteers in Phase 1/2 ANCHOR. October 5 is the announcement date; dosing began in September.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-05$BLFSBioLife Solutions / RepligenBioLife shareholder vote on Repligen merger, 09:00 ET / 15:00 Europe/Rome. Closing remains conditional.HISTORICAL · Outcome unverifiedPrimary source
2026-10-05$VTVTvTv Therapeutics Inc.Completion of CATT1 Phase 3 enrollment announced October 5: 166 randomized participants with type 1 diabetes; no new efficacy results.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-05$STOKSTOKE THERAPEUTICS INCCompletion of FDA meeting on zorevunersen Dravet-syndrome development announced October 5; actual meeting day not disclosed. Company reports alignment on submission approach, not approval.HISTORICAL · Reported outcomePrimary source
2026-10-05$RZLTRezolute, Inc.FDA recommendation to request a Type B pre-BLA meeting announced October 5; no meeting date or approvability conclusion. sunRIZE missed prespecified primary and key secondary endpoints; BLA strategy awaits upLIFT results.HISTORICAL · Reported outcomePrimary source
2026-10-05$RVMDRevolution Medicines, Inc.First patients treated in Phase 3 RASolute 309 announced October 5: daraxonrasib plus zoldonrasib in first-line metastatic RAS G12D pancreatic adenocarcinoma. Actual dosing days not disclosed; no approval of this combination.HISTORICAL · Reported outcomeCompany release
Trial registry
2026-10-05$RADXRadiopharm Theranostics LimitedCompletion of RAD101 end-of-Phase-2 FDA meeting for brain-metastasis imaging announced October 5; actual meeting day unspecified. Formal minutes expected in approximately 30 days, not a fixed deadline or Phase 3 initiation.HISTORICAL · Reported outcomePrimary source
2026-10-05$PRMEPrime MedicineFirst patient dosed in Phase 1/2 PM577a for H1069Q-mutated Wilson disease, announced October 5; actual dosing day not disclosed.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-05$PCVXVAXCYTE INCOPUS-1 pivotal adult Phase 3 topline reported October 5: all prespecified primary endpoints met. Individual PCV21 comparisons met the >0.667 criterion for 17/19 serotypes; all 19 met the historical >0.5 threshold.HISTORICAL · Reported outcomePrimary source
2026-10-05$LSTALisata Therapeutics, Inc.Marea, a Lisata subsidiary, announced first patient dosed in Phase 2 MAR002 for acromegaly October 5; actual dosing day not disclosed.HISTORICAL · Reported outcomePrimary source
2026-10-05$COYACoya Therapeutics, Inc.ALSTARS Phase 2/3 ALS trial reached the target of 120 enrolled participants, announced October 5; additional eligible patients already screening may still enroll.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-05$BEATHeartBeamFDA Breakthrough Device Designation for at-home assessment of potential heart attacks announced October 5. This designation is not clearance for myocardial-infarction assessment; future pivotal development and regulatory submission are still required.HISTORICAL · Reported outcomePrimary source
2026-10-05$ALVOALVOTECHFDA approval of AVT02/SIMLANDI BLA supplement for a second Reykjavik drug-substance suite announced October 5. Other pending product BLAs remain subject to individual reviews; this is not approval of those applications.HISTORICAL · Reported outcomePrimary source
2026-10-05$ALECAlectorGlobal license with Genentech for preclinical brain-penetrant GCase AL050 announced October 5; agreement dated September 30. $100 million upfront; contingent milestones are not guaranteed. Parkinson’s and other neurodegenerative diseases.HISTORICAL · Reported outcomePrimary source
Supporting source
2026-10-03$GMABGenmab A/SRina-S Phase 2 RAINFOL-01 Part C data in platinum-resistant ovarian cancer reported: 109 patients, 45.9% objective response rate and 12.1-month median response duration. Single-arm data, not randomized comparative evidence.HISTORICAL · Reported outcomePrimary source
2026-10-03$AGENAgenus Inc.IGCS Phase 1b recurrent ovarian-cancer cohort update reported: estimated three-year overall survival 48% in 35 efficacy-evaluable patients. Small nonrandomized cohort; not comparative proof.HISTORICAL · Reported outcomePrimary source
2026-10-02$SRZNSurrozenSZN-8141 IND became effective for diabetic macular edema, announced October 2, enabling clinical development; not marketing approval.HISTORICAL · Reported outcomePrimary source
2026-10-02$NVONovo NordiskExtended denecimig BLA review for hemophilia A with/without inhibitors announced due to manufacturing-facility remediation. No new FDA action timeline and no clinical efficacy/safety deficiencies reported by the company. This is not a CRL.HISTORICAL · Reported outcomePrimary source
2026-10-02$LLYEli Lilly and CompanyFDA approved pirtobrutinib for previously untreated adult CLL/SLL with no known 17p deletion.HISTORICAL · Reported outcomePrimary source
Trial registry
2026-10-02$BIIBEisai Inc.52-week Phase 2 AMETHYST Part A data in cutaneous lupus erythematosus reported at EADV; separate from the blinded Phase 3 portion.HISTORICAL · Reported outcomePrimary source
2026-10-01$REGNRegeneron PharmaceuticalsRegeneron and Sanofi expanded their collaboration to four long-acting immunology antibodies, including Phase 1 REGN20423 for atopic dermatitis. Regeneron is to receive $1 billion upfront and may earn up to $7 billion in milestones; costs and future profits shared equally. Agreement announcement, not confirmation of cash receipt.HISTORICAL · Reported outcomePrimary source
Supporting source
2026-10-01$GLUEMonte Rosa Therapeutics, Inc.GFORCE-1 Phase 1 data reported October 1. Biomarker reductions do not establish clinical cardiovascular benefit.HISTORICAL · Reported outcomePrimary source
2026-10-01$FHTXFoghorn TherapeuticsCompany announced it will not advance FHD-909 to expansion after Phase 1 and will not advance the selective SMARCA2 degrader collaboration. Development discontinuation, not FDA rejection.HISTORICAL · Reported outcomePrimary source
2026-10-01$CGEMCullinan Therapeutics, Inc.RTOR NDA submission initiated for zipalertinib plus chemotherapy in previously untreated EGFR exon20ins NSCLC. Separate from the second-line monotherapy NDA with February 27, 2027 PDUFA.HISTORICAL · Reported outcomePrimary source
Aug 12, 2026 — announcement$ALTAltimmune, Inc.RESTORE Phase 2 enrollment completed in July 2026; announcement August 12Exact July completion day not disclosed. This row uses the announcement date; the H2 2027 topline is a separate future milestone.HISTORICAL · Completed eventPrimary source
Sep 21, 2026$NAMSNewAmsterdam PharmaUbeslo / Evlarco: European Commission authorizationEU authorization announced September 21.HISTORICAL · Completed eventPrimary source
$GRALGRAILGalleri — multi-cancer early detection test for adults aged 50 and overOn September 23, the advisory panel voted 7–2 with one abstention that benefits outweigh risks; safety 10–0; effectiveness 6–4, according to GRAIL. The vote is nonbinding. FDA review of the Galleri PMA continues; this is not approval.HISTORICAL · FAVORABLE ADCOM — FDA PENDINGGRAIL · FDA
Sep 23, 2026$ARCTArcturus TherapeuticsARCT-810 Phase 2 interim results and LUNAR 2.0 update releasedResults released September 23 with a webcast. ARCT-2601 integration is a separate future milestone.HISTORICAL · Completed eventPrimary source
2026-09-24$MRKMerck & Co.Belzutifan plus lenvatinib FDA-approved September 24; former October 4 target resolved.HISTORICAL · FDA approvedPrimary source
$MIRMMirum PharmaceuticalsAtebrioz (zilurgisertib)FDA lists approval on September 25, 2026 for reducing new heterotopic ossification in adults and patients aged 12 and older with FOP. Former September 26 PDUFA target resolved; licensed from Incyte.HISTORICAL · FDA APPROVEDFDA
2026-09-25$MRKMerck & Co.Ifinatamab deruxtecan BLA voluntarily withdrawn September 25; former October 10 target superseded. Phase 3 continues.HISTORICAL · Application withdrawnPrimary source
2026-09-28$KODKodiak SciencesDAYBREAK: Zenkuda and KSI-501 met vision non-inferiority primary endpoints versus aflibercept; sponsor topline September 28. Zenkuda 54% at 24-week dosing. Not FDA approval.HISTORICAL · Results publishedPrimary source
Sep 24, 2026$KYTXKyverna Therapeutics, Inc.Phase 2 longer-term miv-cel follow-up in generalized myasthenia gravis released September 24, 2026. The former Q3 window is resolved.HISTORICAL · Results releasedPrimary source
Sep 24, 2026$KYTXKyverna Therapeutics, Inc.One-year miv-cel topline in stiff person syndrome released September 24, 2026. The former Q3 window is resolved.HISTORICAL · Results releasedPrimary source
Sep 24, 2026$ACADAcadia Pharmaceuticals Inc.Phase 2 remlifanserin topline released September 24, 2026. Primary endpoint missed statistical significance (p=0.0603); Phase 3 continuation planned with protocol amendments.HISTORICAL · Results releasedPrimary source
2026-09-28$ACETAdicet Bio, Inc.Prula-cel Phase 1 clinical data released in SLE/LN.HISTORICAL — Results releasedPrimary source
2026-09-28$MIRMMirum PharmaceuticalsAZURE-1 Phase 3 brelovitug topline released; primary endpoint met.HISTORICAL — Results releasedPrimary source
2026-09-29$IVVDInvivyd, Inc.LIBERTY Phase 3 VYD2311 safety/tolerability topline released; distinct DECLARATION study remains pending.HISTORICAL — Results releasedPrimary source
Q3 2026$IVVDInvivyd, Inc.Prior combined LIBERTY/DECLARATION forecast superseded by separate company updates on 29 September.HISTORICAL — Superseded forecastPrimary source
2026-09-28$IVAInventiva S.A.First-half 2026 financial results published; conference call announced for 08:00 ET.HISTORICAL — Results releasedPrimary source
2026-09-28$IMMPImmutep LimitedAnnounced ADS-ratio change.HISTORICAL — Execution unverifiedPrimary source
2026-09-28$SABSSAB BiotherapeuticsSAB-142 Phase 1 presentation scheduled at EASD.HISTORICAL — Occurrence unverifiedPrimary source
2026-09-29$KYTXKyverna TherapeuticsKYSA-6 Phase 2 follow-up presentation scheduled at AANEM.HISTORICAL — Occurrence unverifiedPrimary source
$SRPTSarepta TherapeuticsWMS Duchenne data presentationsScheduled scientific presentation, not an automatic pivotal readout. Stock HubHISTORICAL — Occurrence unverifiedPrimary source
Sep 30, 2026$INCYIncyte CorporationSTOP-HS Phase 3 povorcitinib posters at EADV 2026. Incyte lists two povorcitinib STOP-HS1/STOP-HS2 Phase 3 poster abstracts for the EADV 2026 session on 30 September 2026 at 07:00 CEST, covering acne and high-disease-burden analyses. This is a congress presentation of additional analyses, not a new topline readoutHISTORICAL — Occurrence unverifiedPrimary source
Sep 30, 2026$INCYIncyte CorporationTRuE-AD4 ruxolitinib cream poster at EADV 2026. Incyte lists the TRuE-AD4 poster on ruxolitinib cream in moderate atopic dermatitis for the EADV 2026 session on 30 September 2026 at 07:00 CEST. This is a congress presentation, not a new pivotal topline readoutHISTORICAL — Occurrence unverifiedPrimary source
Sep 30, 2026$SABSSAB Biotherapeutics, Inc.three SAB-142 Phase 1 presentations at EASD 2026HISTORICAL — Occurrence unverifiedPrimary source
Oct 1, 2026 · 16:30 CEST$NKTRNektar TherapeuticsREZOLVE-AA Phase 2b 52-week rezpegaldesleukin data oral presentation at EADVPresentation 16:30-16:40 CEST, Hall N, abstract AS-1872; conference discussion of previously reported data.HISTORICAL — Results releasedPrimary source
Oct 1, 2026 · 10:25 CEST$NKTRNektar TherapeuticsREZOLVE-AD Phase 2b maintenance rezpegaldesleukin data oral presentation at EADVPresentation 10:25-10:35 CEST, Hall N, abstract AS-1732; distinct from initial topline.HISTORICAL — Results releasedPrimary source
Oct 1, 2026 · session 16:30–18:00 CEST$ARTVArtiva Biotherapeutics, Inc.AlloNK (AB-101) plus rituximab Sjogren disease clinical data presentation at ISSjDConfirmed presentation day. Session 16:30-18:00 CEST; individual talk time unspecified. Data from 11 patients; not a Phase 3 RA readout.HISTORICAL — Results released; oral session unverifiedPrimary source
Oct 1, 2026 · 16:30 CEST$EVMNEvommune, Inc.EVO301 Phase 2a atopic dermatitis late-breaking data presentation at EADV16:30-16:45 CEST, Hall A. Topline was already released in February; this is a conference presentation.HISTORICAL — Occurrence unverifiedPrimary source
Oct 2, 2026$SANASana Biotechnology, Inc.UP421 clinical-data symposium at EASD 2026Presentation day confirmed; no presentation time inferred.HISTORICAL — Occurrence unverifiedPrimary source
$TRDAEntrada TherapeuticsENTR-601-44 pharmacokinetic / pharmacodynamic translation presentation at WMSScientific presentation; not assumed to be a new patient efficacy readout. Stock HubHISTORICAL — Occurrence unverifiedPrimary source
Sep 27–30, 2026 (conference)$BIAFbioAffinity Technologies, Inc.CyPath Lung posters at NAVREF 2026The individual poster presentation days have not been announced.HISTORICAL — Occurrence unverifiedPrimary source
2026-09-29$QUREuniQure N.V.uniQure released the four-year (48-month) Phase I/II data for AMT-130 (ifezuntirgene inilparvovec) in Huntington's disease on September 29, 2026. In 12 high-dose patients at 48 months, cUHDRS showed 44% slowing of disease progression versus an updated external control (not statistically significant, p=0.144) and TFC showed 61% slowing (nominal p=0.008); an updated 36-month analysis of 15 high-dose patients showed 80% slowing on cUHDRS (nominal p=0.005) and 67% on TFC (nominal p=0.011).HISTORICAL · Disclosed eventSEC filing
SEC filing
Supporting source
Q3 2026$CRMDCorMedix TherapeuticsREZZAYO prophylaxis sNDA submissionCompany-guided submission window.HISTORICAL — Estimate expired; outcome unverifiedPrimary source
2026-09-30$MLTXMoonLake ImmunotherapeuticsMoonLake submitted a BLA to the FDA on September 30, 2026 for sonelokimab in moderate-to-severe hidradenitis suppurativa in adults and pediatric patients 12 years of age and older. The company expects to learn whether the BLA is accepted for review within about 60 days of submission, and to receive the planned review timeline within about 74 days.HISTORICAL · Disclosed eventSEC filing
Supporting source
Supporting source
Sep 30, 2026$BMYBristol Myers SquibbCAMZYOS (mavacamten): FDA approved pediatric oHCM expansion for patients weighing at least 30 kg.HISTORICAL — FDA approvedPrimary source
September 29 to October 3, 2026$CAPRCapricor Therapeutics, Inc.Deramiocel HOPE-3 and HOPE-3 OLE presentations at WMS 2026HOPE-3 oral presentation is confirmed October 3. Late-breaking HOPE-3 OLE poster day is not specified by this release. Conference in Hiroshima, Japan.Conference rangePrimary source

The Tracker shows a curated feed of upcoming catalysts and open windows; the Calendar also retains history. The AI Lookup searches the web for current information on the complete ticker universe, including tickers with only historical events. ClinicalTrials.gov data-collection dates are not results-publication dates. Windows and deadlines can change. Educational information only; not financial advice.

The free Biotech Catalyst Calendar combines an embedded archive with a sourced selection of regulatory deadlines, clinical readouts, congress presentations and company milestones. Exact dates and estimated windows are labeled separately; completed events remain in history.

The page also includes a glossary covering key FDA, clinical trial, and catalyst terminology, including regulatory designations, trial progress stages, and common clinical metrics. All data is sourced from public information and may contain errors or estimated dates; users are advised to verify with official sources before making any decisions.

Biotech Catalyst Lookup

Type a ticker to get an AI-generated snapshot of the next catalyst (PDUFA, clinical data, regulatory events) with a link to the primary source.

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Dates, events and sources may be incomplete, incorrect or out of date. Check the information against official company releases, SEC filings, FDA documents or ClinicalTrials.gov. Estimated dates are not firm deadlines.

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Recently viewed catalysts

DRTSClinical
Alpha Tau Medical Ltd. (Nasdaq: DRTS)
Presentation of new REGAIN trial data (safety interim analysis) at the 31st Annual Meeting of the Society for Neuro-Oncology (SNO) 2026, Philadelphia
2026-11-13
CRBPClinical
Corbus Pharmaceuticals Holdings, Inc. (NASDAQ: CRBP)
Late-breaking presentation of CANYON-1 Phase 1b efficacy, safety and tolerability data at ObesityWeek 2026
2026-11-15
VKTXClinical
Viking Therapeutics, Inc.
VANQUISH-1 and VANQUISH-2 Phase 3 topline results for subcutaneous VK2735 in obesity (not yet announced)
2027
SRPTPDUFA
Sarepta Therapeutics, Inc.
FDA target action date for supplemental applications seeking traditional approval of AMONDYS 45 (casimersen) and VYONDYS 53 (golodirsen)
2027-02-28
IBRXData readout
ImmunityBio, Inc.
Topline results from QUILT-2.005 Cohort A, a registrational trial of ANKTIVA plus BCG versus BCG alone in BCG-naive non-muscle-invasive bladder cancer
November 2026
SENSCatalyst
Senseonics Holdings, Inc.
Commercial launch of the integrated Eversense 365 and Beta Bionics iLet Bionic Pancreas system
Q4 2026
NKTRClinical
Nektar Therapeutics
Initiation of the Phase 3 ZENITH AA study of rezpegaldesleukin in severe-to-very-severe alopecia areata
early 2027
ROIVRegulatory
Roivant Sciences Ltd. (Nasdaq: ROIV)
Planned supplemental New Drug Application (sNDA) submission for brepocitinib in non-infectious uveitis (NIU)
first half of calendar year 2027
BHVNPDUFA
Biohaven Ltd. (NYSE: BHVN)
FDA action on the resubmitted new drug application for Vyglxia (troriluzole) in spinocerebellar ataxia (SCA), with a user fee goal date in the first quarter of 2027; an advisory committee meeting is also planned with date to be announced
first quarter of 2027
ABOSClinical
Acumen Pharmaceuticals, Inc. (ABOS)
Topline results from the Phase 2 ALTITUDE-AD trial of intravenous sabirnetug in early Alzheimer's disease
late 2026
IMRXClinical
Immuneering Corporation (IMRX)
Topline data from the pivotal Phase 3 MAPKeeper 301 trial of atebimetinib plus mGnP in first-line metastatic pancreatic cancer
mid-2028
TGTXClinical
TG Therapeutics, Inc.
Topline Phase 3 data for subcutaneous BRIUMVI (ublituximab-xiiy) in relapsing multiple sclerosis
year-end 2026 or Q1 2027 (company window; no exact day announced)

Catalyst Calendar Glossary

Quick definitions for FDA, clinical-trial, and “catalyst” terms used in the calendar & trackers.

1) FDA / Regulatory

TermMeaning
PDUFA dateFDA target action date for an NDA/BLA decision (often disclosed via filings/press releases).
Priority ReviewFDA review goal generally 6 months; the clock depends on the application type. It does not guarantee approval or a decision on a fixed date.
Standard ReviewFDA review goal generally 10 months; clock start and pathway depend on the application.
AdComAdvisory committee: reviews evidence and may vote; a meeting does not imply approval and its advice is not binding on FDA.
NDA / BLAApplications to approve a drug (NDA) or a biologic (BLA).
sNDA / sBLASupplemental application (label expansion, new population, new formulation, etc.).
Filing acceptanceFDA accepts the application as sufficiently complete to start review (often when PDUFA is set).
RTF (Refuse-to-File)FDA declines to accept an application for review (formal/technical deficiencies).
CRL (Complete Response Letter)FDA does not approve at that time and requests additional info/changes before resubmission.
Resubmission (Class 1 / Class 2)Re-file after CRL; Class 1 = minor changes (often shorter), Class 2 = major (often longer).
PDUFA delay/extensionFDA pushes the action date (more time needed for review, inspections, analyses, etc.).

2) FDA Meetings

TermMeaning
Type AUrgent/critical meeting (clinical hold, disputes, time-sensitive issues).
Type BStandard “milestone” meeting (End-of-Phase, pre-NDA/BLA, etc.).
Type COther focused meeting on specific topics; can still be strategically important.
EOP (End-of-Phase)Aligns requirements to move forward (next phase / registrational plan / filing path).
SPASpecial Protocol Assessment: FDA agrees in advance on design/endpoint of a key trial (not a guarantee).

3) Trial Progress vs Data Release

TermMeaningData released?
Enrollment InitiationFirst sites/patients start enrolling.NO
Enrollment CompleteEnrollment finished (no more new patients).NO
Trial CompletedFinal protocol-defined data collection completed. Primary completion concerns primary outcomes; study completion includes secondary outcomes and adverse events. Neither means results have been published.NO
Database LockDataset is finalized for analysis (internal milestone).NO
Interim DataResults from an interim analysis, which may remain internal. They count as released data only when publicly disclosed.IF DISCLOSED
Topline DataHigh-level results release (often via PR/filing).YES
Data Released / ReadoutResults publicly disclosed; internal analysis alone does not constitute a public readout.YES
Full Results / Full DatasetDetailed results published or presented; does not necessarily mean access to the full raw dataset.YES
Conference PresentationAbstract, poster or oral presentation. A scheduled slot alone does not establish that new results have been released.IF DISCLOSED
PublicationPeer-reviewed paper / full write-up.YES
Key rule: “Trial Completed” ≠ “Data Released”. Completion is an operational milestone; data can come weeks/months later.

4) Common Clinical Metrics

TermMeaning
OSOverall Survival.
PFSProgression-Free Survival.
ORRObjective Response Rate (CR + PR).
CR / PRComplete / Partial Response.
SD / PDStable Disease / Progressive Disease.
DORDuration of Response.
AE / SAEAdverse event / serious adverse event under regulatory criteria, such as death, life-threatening events or hospitalization. Seriousness differs from severity of intensity; causation is not automatic.
PK / PDPharmacokinetics / Pharmacodynamics.
BiomarkerBiological marker used for selection/response/target engagement.

5) “Accelerators” / Designations

TermMeaning
ODDOrphan Drug Designation (rare-disease incentives).
FTDFast Track Designation (more frequent interactions; potential rolling submission).
BTDBreakthrough Therapy Designation: preliminary clinical evidence of potential substantial improvement on clinically significant endpoints over available therapies for a serious condition. It is not approval.
RMATDesignation for eligible regenerative therapies, including certain cell, tissue and gene therapies, with preliminary clinical evidence of potential to address unmet needs in serious conditions. It is not approval.
RPDD / PRVRPDD is a rare pediatric disease designation. A PRV is a separate voucher that may be awarded with a qualifying approval and transferred or used to request priority review of another application. Designation guarantees neither a voucher nor approval.

6) Calendar Fields (how to read them)

FieldMeaning
StageProgram phase (Preclinical, Phase 1/2/3, NDA/BLA Filing, PDUFA, etc.).
StatusOperational status (Ongoing, Trial Completed, Data Released, Clinical Hold, etc.).
Next catalystNext expected milestone (Topline, Interim, Conference, Submission, Regulatory Decision).
Catalyst dateDate or time window (exact / month / quarter / half / year / range).

Glossary sources: FDA BTD · FDA RMAT · FDA RPDD/PRV · FDA SAE · ClinicalTrials.gov

Related research

Methodology

Stock Hub follow-up, September 27, 2026: 18 missing events added for CGEM, TRDA, SRPT, ORKA and PRAX, checked against sponsor or SEC disclosures. Existing relutrigine and EVERLAST entries were preserved. Scheduled scientific presentations are distinguished from new efficacy readouts; company windows remain estimates. This targeted addition does not re-verify unrelated archive entries.

Sources: FDA documents, SEC filings, sponsor releases and ClinicalTrials.gov. The September 27, 2026 review integrates 49 new or recovered future milestones, updates ACET, ACIU, XENE and CAPR, and separates completed events into history. Other entries retain earlier September 19–26 checks; this update does not re-certify every archive entry. The embedded calendar may include historical events and estimated windows. Registry dates concern data collection, not necessarily public readouts. Stated times include their timezone; EDT is New York daylight time and CEST is daylight time in Italy.

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Important Disclaimer

The dates and events shown in this calendar are collected from publicly available sources and company communications, but may change at any time and may contain errors, inaccuracies, delays or omissions. Some dates are estimated, some timelines may be revised, and certain catalysts may be postponed, cancelled or updated without notice. Always verify with official press releases, SEC filings and primary company sources before making any trading or investment decision.

This content is for educational and informational purposes only. It is not investment advice and not a recommendation to buy or sell any security. Do your own research and consult a licensed advisor. Full disclaimer: merlintrader.com/disclaimer.