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FDA Clears Path for Sarepta's Duchenne Muscular Dystrophy Gene Therapy

FDA Clears Path for Sarepta's Duchenne Muscular Dystrophy Gene Therapy

HEALTH - 7/29/2025

In a surprising turn of events, the FDA has allowed Sarepta Therapeutics to resume shipments of its gene therapy, Elevidys, for younger Duchenne muscular dystrophy patients who can walk, despite concerns over previous fatalities.

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