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Biomea Fusion Inc (BMEA NASDAQ) stock market data APIs
Biomea Fusion Inc Financial Data Overview
Biomea Fusion, Inc., a clinical-stage diabetes and obesity medicines company, focuses on the discovery and development of oral drugs to treat patients with diabetes and obesity. It's lead clinical program's drug candidates are COVALENT-111 and COVALENT-112, which has completed Phase II clinical trials of icovamenib for the treatment of Type 1 and Type 2 diabetes; COVALENT-211, which is in Phase II clinical trial of icovamenib for treating insulin-deficient type 2 diabetes; and COVALENT-212, which is in Phase II clinical trial of icovamenib for the treatment of type 2 diabetes. The company is also developing BMF-650, which is in Phase I glucagon-like peptide-131 clinical trial for the treatment of obesity. The company was incorporated in 2017 and is headquartered in San Carlos, California.
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Biomea Fusion Inc Fundamental data includes:
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- EBITDA: -63 382 000
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- Latest Release: 2026-04-06
- EPS/Forecast: -0.2302
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Biomea Fusion Inc News
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Biomea Fusion Reports First Quarter 2026 Financial Results and Corporate Highlights
Successfully completed chronic toxicology studies for icovamenib, providing the nonclinical support for advancing to chronic clinical dosing, beyond the 12-week clinical dosing that has been used to d...
Biomea Fusion Announces Poster Presentations of Icovamenib at the American Diabetes Association (ADA) 86th Scientific Sessions
SAN CARLOS, Calif., May 05, 2026 (GLOBE NEWSWIRE) -- Biomea Fusion, Inc. (“Biomea” or “Biomea Fusion” or “the Company”) (Nasdaq: BMEA), a clinical-stage diabetes and obesity company, tod...
Biomea Announces Positive 52-Week Data From Phase 2 COVALENT-112 Trial Of Icovamenib In T1 Diabetes
(RTTNews) - Biomea Fusion, Inc. (BMEA), a clinical-stage diabetes and obesity company, announced positive 52-week results from its Phase 2 COVALENT-112 trial evaluating Icovamenib in patients with typ...
Biomea Fusion Announces Positive 52-Week Results from Phase 2 COVALENT-112 Trial in Type 1 Diabetes Showing C-Peptide Improvement and Durability Following 12-Weeks of Icovamenib Treatment
A 52% increase from baseline in mean C-peptide AUC at Week 12 in patients diagnosed within 0–3 years (n=5) receiving icovamenib 200 mg, with a clear dose response observed vs 100 mg (n=6)Persistence...
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