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Breaking: FDA panel endorses Sarepta's Duchenne gene therapy

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FDA advisory panel narrowly recommends approval for Sarepta's gene therapy for Duchenne

A panel of independent FDA advisers voted 8-6 Friday to recommend accelerated approval for Sarepta's gene therapy for Duchenne muscular dystrophy, ruling that the potential benefit to patients outweighs a long list of concerns from agency reviewers. 

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Friday, May 12, 2023

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