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Sarepta Therapeutics Provides Clarifying Statement on ELEVIDYS

1. FDA investigating death of patient after ELEVIDYS gene therapy. 2. Sarepta confirms death was deemed unrelated to the therapy.

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FAQ

Why Bearish?

The investigation indicates potential safety concerns which can deter investors. Historical instances such as the FDA scrutiny of other gene therapies have led to price declines.

How important is it?

The investigation could reflect poorly on SRPT's products, impacting investor confidence and stock performance.

Why Short Term?

Immediate market reactions to safety concerns typically occur, but longer-term effects depend on further investigation outcomes.

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CAMBRIDGE, Mass.--(BUSINESS WIRE)--Sarepta Therapeutics, Inc. (NASDAQ:SRPT), the leader in precision genetic medicine for rare diseases, today issued the following statement: Just before 6:00 p.m. ET today, the U.S. Food and Drug Administration (FDA) issued a press release announcing an investigation into the death of an eight-year-old Duchenne muscular dystrophy (Duchenne) patient who had received ELEVIDYS (delandistrogene moxeparvovec) gene therapy. The death of this patient was deemed unrela.

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