FDA investigates patient deaths after treatment with Sarepta's gene therapy-February 2024-www.financetom.com

FDA investigates patient deaths after treatment with Sarepta's gene therapy

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FDA investigates patient deaths after treatment with Sarepta's gene therapy

Jun 24, 2025 2:10 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 ) gene therapy, Elevidys.

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