Keros Faces Stock Plunge, Suspends Two Hypertension Study Arms Due to Heart Safety Concerns

Keros Therapeutics experienced a significant decline in its stock price, dropping over 70% during premarket trading after announcing safety concerns related to its hypertension drug candidate, cibotercept[1]. The biotech company was compelled to suspend dosing in the 3-mg/kg and 4.5-mg/kg arms of its Phase II TROPOS trial due to unexpected cases of pericardial effusion, which is an accumulation of fluid around the heart[2]. This adverse development led to a 65% drop in Keros’ shares as the safety issues prompted immediate concern among investors[2]. Truist Securities analysts predict continued pressure on the stock until these safety concerns are fully addressed, with more data expected by the second quarter of 2025[1].
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Explore Further
What specific mechanisms led to the unexpected pericardial effusion cases in the higher dose arms of the cibotercept trial?
How is Keros Therapeutics addressing the safety concerns to regain investor confidence following the stock decline?
What steps are being taken by Keros to ensure patient safety during the ongoing 1.5-mg/kg dosing arm of the trial?
How might the suspension of the cibotercept trial's higher dose arms impact Keros' collaboration with Takeda?
What potential future strategies could Keros employ to mitigate stock volatility caused by clinical trial setbacks?