FDA
approval
· 2021-02-11
FDA Approved: VYONDYS 53 — Supplemental Application (Sarepta Therapeutics, Inc.)
Summary
FDA approved a supplemental application for VYONDYS 53 (golodirsen) from Sarepta Therapeutics, Inc. The approval pertains to Duchenne muscular dystrophy.
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Diseases / indications
Drugs mentioned
Snippet
SUPPL AP for VYONDYS 53 (GOLODIRSEN)