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Biomea Fusion shares hold with Buy rating after trial success

EditorAhmed Abdulazez Abdulkadir
Published 12/18/2024, 08:52 PM
BMEA
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On Wednesday, Biomea Fusion Inc. (NASDAQ:BMEA), a clinical-stage biopharmaceutical company with a market capitalization of $168 million, received a reiterated Buy rating and a $40.00 price target from H.C. Wainwright, following the announcement of positive topline results from its Phase 2 COVALENT-111 clinical trial. The stock, which has declined 68% year-to-date, appears undervalued according to InvestingPro analysis. The trial evaluated the effectiveness of icovamenib in treating patients with type 2 diabetes (T2D) and showed promising outcomes.

The COVALENT-111 trial included adult T2D patients who had been diagnosed within the last seven years and were treated with up to three anti-diabetic medications. Participants had baseline HbA1c levels ranging from 7.0% to 10.5% and a body mass index (BMI) between 25 and 40 kg/m². They were randomized into different dosing arms, with assessments at the 26-week and 52-week marks.

The data revealed that icovamenib led to a statistically significant mean HbA1c reduction when compared to placebo in the per-protocol patient population, which included all dosing arms. The greatest HbA1c reduction of 1.47% was observed in patients with severe insulin-deficient diabetes (SIDD) after a 12-week treatment period with 100 mg dosing. The treatment was also well-tolerated, with no treatment-emergent adverse events (TEAEs) leading to discontinuation, no hypoglycemic events, and no serious adverse events (SAEs).

These topline results suggest that icovamenib could offer an effective option for long-term glycemic control with a short treatment duration. The findings indicate the potential for improved HbA1c reductions after 12 weeks of treatment, particularly in patients with SIDD, which may guide the optimal dose and treatment period for future clinical development. InvestingPro data shows analyst targets ranging from $11 to $128, reflecting diverse views on the company's potential.

Biomea Fusion plans to continue analyzing the full dataset from the COVALENT-111 trial and expects to present further results at a medical conference in 2025. The company also anticipates reporting the 52-week results in the second half of 2025. The reiteration of the Buy rating and the $40 price target reflect confidence in the drug's clinical progress and potential market impact. According to InvestingPro, the company maintains a strong liquidity position with more cash than debt and a current ratio of 3.39, though it's currently burning through cash. Subscribers can access 10+ additional ProTips and comprehensive financial analysis in the Pro Research Report.

In other recent news, Biomea Fusion Inc. has seen significant developments in its business operations. The company reported its third-quarter earnings for 2024, concluding with $88.3 million in cash and equivalents. Piper Sandler raised the stock price target for Biomea Fusion to $19.00, maintaining an Overweight rating. EF Hutton also issued a Buy rating for the company, setting a price target of $128.00, while H.C. Wainwright maintained its Buy rating with a $40.00 price target. Truist Securities upgraded the company's stock from Hold to Buy.

Biomea Fusion's investigational drug, icovamenib, received global and US naming approval from the World Health Organization and the USAN Council. The company also announced the formation of its Global Scientific Advisory Board, composed of international experts in diabetes and beta cell science. Biomea Fusion is expected to release preclinical safety and efficacy data for a new obesity drug candidate.

These are recent developments in the company's operations. Biomea Fusion is currently conducting Phase I/II and Phase II clinical trials for icovamenib, with top-line readouts expected in December. The company also plans to advance the clinical development of icovamenib using their proprietary FUSION™ System. The U.S. Food and Drug Administration (FDA) has lifted the clinical hold on icovamenib studies, allowing the company to continue its clinical trials.

This article was generated with the support of AI and reviewed by an editor. For more information see our T&C.

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