Biomea reported 52-week follow-up results from the Phase II COVALENT-111 trial of icovamenib in adults with type 2 diabetes at the ATTD conference. The double-blind, randomized, placebo-controlled study tested 100 mg once daily for 8 weeks, 100 mg once daily for 12 weeks, or 8 weeks once daily followed by 4 weeks twice daily. In severe insulin-deficient diabetes patients, the 12-week once-daily arm showed a mean HbA1c reduction of 1.5% at Week 52 versus placebo. In participants on GLP-1-based therapy at entry, icovamenib was associated with a 1.2% HbA1c reduction at Week 52 versus placebo. Biomea said 52-week follow-up data from type 1 diabetes patients in COVALENT-112 are expected in Q2 2026.
Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Biomea Fusion Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202603140430PRIMZONEFULLFEED9672005) on March 14, 2026, and is solely responsible for the information contained therein.
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