FDA investigates patient deaths after treatment with Sarepta's gene therapy
ReutersJun 24, 2025 8:54 PM
June 24 (Reuters) - The U.S. Food and Drug Administration said on Tuesday that it is investigating reports of two deaths due to acute liver failure in non-ambulatory Duchenne muscular dystrophy patients after receiving Sarepta Therapeutics' SRPT.O gene therapy, Elevidys.
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