Vyondys package insert

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Actual: Individual is using another exon skipping agent for DMD (including but not limited to Exondys 51, Vyondys 53); OR, Amondys 45 [package insert]
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Vyondys 53 is indicated for the treatment of Duchenne muscular dystrophy (DMD) in Package Insert - ELEVIDYS (fda.gov). Revised 10/2024. Member

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by UMP Subcommittee 2024Elevidys in accordance to the package insert for Elevidys (See Appendix A for Vyondys 53 intravenous infusion [prescribing information].

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Vyondys 53 [package insert]. Cambridge, MA: Sarepta Therapeutics, Inc.; March 2024. 2. Clinical Pharmacology [database online]. Tampa, FL

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Viltepso [package insert], Paramus, NJ: NS Pharma, Inc.; March 2024. Vyondys 53 [package insert], Cambridge, MA: Sarepta Therapeutics

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(Vyondys 53), viltolarsen (Viltepso)), or Casimersen (Amondys 45) ​are Per the Amondys 45 package insert, Amondys 45 was approved by the FDA under

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Vyondys 53 while maintaining optimal therapeutic outcomes. References. 1. Vyondys 53 [package insert]. Cambridge, MA: Sarepta Therapeutics

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Amondys 45, Exondys 51. Vyondys 53, Viltepso) after Elevidys PACKAGE INSERT INFORMATION: INDICATION, AGE, DOSE, AND ANY. PRE

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Vyondys 53; new prior authorization for Vyondys 53. Coding Reviewed Package inserts. U.S. National Library of Medicine, National

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Vyondys 53 [package insert]. Cambridge, MA. Sarepta Therapeutics, Inc. December 2024. 3. Viltepso [package insert]. Paramus, NJ; NS Pharma; August 2024

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