
Bristol-Myers Squibb (BMY) received a reiterated "Market Perform" rating and $58 price target from Bernstein SocGen Group after discontinuing its Phase 3 Milvexian ACS trial due to efficacy concerns, raising risks for upcoming Milvexian trials in Secondary Stroke Prevention, though the Atrial Fibrillation trial shows potential with a different dosing strategy. Despite this pipeline setback, BMY maintains strong fundamentals, including a 5.32% dividend yield and perceived undervaluation, while also expanding cancer research collaborations and completing a €5 billion bond offering.
Bristol-Myers Squibb (BMY) faces increased pipeline risk following the discontinuation of its Phase 3 Milvexian ACS trial due to efficacy concerns, prompting Bernstein SocGen Group to reiterate a "Market Perform" rating with a $58 price target. This setback specifically elevates concerns for the Secondary Stroke Prevention (SSP) trial, which shares a similar dosing regimen to the failed ACS study, while the Atrial Fibrillation (AF) trial, with its more aggressive 100mg BID dosing, is viewed as a potential bright spot aiming for non-inferiority against Eliquis. Despite the Milvexian challenge, BMY exhibits strong underlying fundamentals, including a 5.32% dividend yield maintained for 55 consecutive years, and is considered undervalued by InvestingPro at its current trading price of $46.65. The company has also strategically expanded its collaboration with Sarah Cannon Research Institute for cancer therapy development and successfully priced a €5 billion senior unsecured note offering. Upcoming catalysts include results from the two remaining Milvexian Phase 3 trials in 2026 and new efficacy data for Camzyos, expected at the American Heart Association's Scientific Sessions in 2025. These developments highlight BMY's diversified pipeline efforts and financial stability, which could mitigate the impact of the recent trial failure.
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