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Sarepta Moves Closer To FDA Approval For Duchenne Muscular Dystrophy Drugs

BenzingaVandana Singh

FDA accepts Sarepta's filings seeking traditional approval for AMONDYS 45 and VYONDYS 53, with a decision expected by February 2027.

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  1. SEC EDGARSEC EDGAR

    8-K filing — Sarepta Therapeutics, Inc. (SRPT)

    Filed: 2026-07-27 AccNo: 0001193125-26-316995 Size: 334 KB Item 5.02: Departure of Directors or Certain Officers; Election of Directors; Appointment of Certain Officers: Compensatory Arrangements of Certain Officers Item 7.01: Regulation FD Disclosure Item 9.01: Financial Statements and Exhibits