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FDA approval · 2021-02-11

FDA Approved: VYONDYS 53 — Supplemental Application (Sarepta Therapeutics, Inc.)

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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

  • VYONDYS 53 (golodirsen)

Snippet

SUPPL AP for VYONDYS 53 (GOLODIRSEN)