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OLMA US Equity

Olema Pharmaceuticals, Inc.Health Care · Pharmaceutical Preparations · CIK 1750284 · FY ends Dec 31
$10.65
-0.12 (-1.11%)
USD · as of 2026-08-18 · marketstack
6 registered studies · 5 active

Studies where OLMA is the lead sponsor, as filed with ClinicalTrials.gov. Completion dates are the sponsor's own projected windows and are revised as a study runs. Active studies first, then completed and stopped — newest readout first within each.

6 interventional · 1 with posted results

Held by 10 tracked-famous managers (TWO SIGMA INVESTMENTS, LP, Point72 Asset Management, L.P., Duquesne Family Office LLC, Qube Research & Technologies Ltd, CITADEL ADVISORS LLC, +5 more) · FINRA short interest 18.2 days to cover (settled 2026-07-31) · government filings 180d: none disclosed

StudyPhaseStatusInterventionsConditionsEnrollmentPrimary completionReadout inUpdated
Palazestrant in Combination With Ribociclib for the First-line Treatment of ER+/HER2- Advanced Breast CancerNCT07085767Progression-Free Survival (PFS)Randomized · Triple-masked · TreatmentPhase 3RecruitingDrug: Palazestrant, Letrozole-matching placebo, Ribociclib, Letrozole, Palazestrant matching-placeboBreast Cancer, Locally Advanced Breast Cancer, Metastatic Breast Cancer, ER Positive Breast Cancer, HER2 Negative Breast Carcinoma1,000Dec 2028≤ 865 d2026-08-17
Phase 1b Study of OP-1250 (Palazestrant) in Combination With Ribociclib, Alpelisib, Everolimus, or Atirmociclib in ER+, HER2- Breast CancerNCT05508906Dose Limiting Toxicities (DLTs)Non-randomized · Open-label · TreatmentPhase 1RecruitingDrug: Palazestrant, Ribociclib, Alpelisib, Everolimus, AtirmociclibMetastatic Breast Cancer, ER-positive Breast Cancer, HER2-negative Breast Cancer, Breast Cancer, Locally Advanced Breast Cancer1902027-12-31in 499 d2025-10-22
Phase 1 Study of OP-3136 in Advanced or Metastatic Solid TumorsNCT06784193Number of participants with dose-limiting toxicities in the Dose Escalation ArmsRandomized · Open-label · TreatmentPhase 1RecruitingDrug: OP-3136, Fulvestrant, PalazestrantAdvanced or Metastatic ER+ HER2- Breast Cancer (mBC), Advanced or Metastatic Non-Small Cell Lung Cancer (NSCLC), Advanced or Metastatic Castration-Resistant Prostate Cancer (mCRPC), Metastatic Breast Cancer, Fulvestrant, Palazestrant1802027-05-30in 284 d2025-10-10
OP-1250 (Palazestrant) vs. Standard of Care for the Treatment of ER+/HER2- Advanced Breast CancerNCT06016738Dose-Selection Part: Incidence of adverse eventsRandomized · Open-label · TreatmentPhase 3Active, not recruitingDrug: Palazestrant, Fulvestrant, Anastrozole, Letrozole, ExemestaneBreast Cancer, Advanced Breast Cancer, Metastatic Breast Cancer, ER Positive Breast Cancer, HER2 Negative Breast Carcinoma5102026-10-31in 73 d2026-08-13
A Phase 1 Study of Oral OP-1250 in Combination With Palbociclib in HR+/HER2- Breast Cancer PatientsNCT05266105Incidence of Dose Limiting ToxicitiesNon-randomized · Open-label · TreatmentPhase 1Active, not recruitingDrug: Palazestrant, PalbociclibBreast Cancer60Mar 20262025-11-24
A Dose Escalation/Expansion Study of Oral OP-1250 in Subjects With Advanced and/or Metastatic HR+, HER2- Breast CancerNCT04505826results2026-05-11Dose Limiting Toxicities (DLT)Non-randomized · Open-label · TreatmentStudy Protocol · Statistical Analysis PlanPhase 1/2CompletedDrug: OP-1250Hormone Receptor Positive Breast Carcinoma, HER2-negative Breast Cancer1532024-07-30actual2026-05-11

Primary completion is the date the sponsor filed with the registry — their own projection, revised whenever they revise it, unless the row is marked actual.

Source: ClinicalTrials.gov, retrieved 2026-08-19