Duchenne Muscular Dystrophy (DMD)
Summary
Amondys 45 (casimersen), Exondys 51 (eteplirsen), Viltepso (viltolarsen), and Vyondys 53 (golodirsen) are considered investigational for the treatment of Duchenne muscular dystrophy because there is insufficient evidence of clinical benefit. Elevidys (delandistrogene moxeparvovec-rokl) is considered not medically necessary for DMD in ambulatory individuals who have a confirmed DMD gene mutation, as there is insufficient evidence to demonstrate clinical efficacy. The 02/24/2026 review removed the investigational statement for Elevidys in non-ambulatory individuals.
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