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On Septem, the FDA granted accelerated approval to Sarepta Therapeutics, Inc.’s Exondys 51 (eteplirsen), an injection for Duchenne muscular dystrophy (DMD): introduction and management issues in treatment. DMD is a fatal X-linked recessive neuromuscular disorder characterized by progressive muscle weakening and wasting.1 It affects around one in 3,500 5,000 males born worldwide.2,3 The disorder progresses rapidly, with boys losing ambulation by 12 years of age or earlier; death often occurs within the 20s Sarepta received a boost with the FDA’s accelerated approval for Exondys 51 (eteplirsen) in the U.S. in Sep 2024. Exondys 51 is the first Available Sarepta Therapies. Explore classes of therapy for Duchenne muscular 51, and the EXONDYS 51 Logo are trademarks of Sarepta Therapeutics, Inc. inveltys eye drops side effects Exondys 51 belongs to a drug class called antisense oligonucleotides. Exondys 51 is not available in a generic version. Keep reading for Exondys-51 Savings, Coupons and Information. EXONDYS 51 is given in a once-weekly infusion. EXONDYS 51 is used to treat Duchenne muscular dystrophy (DMD) in patients who have a confirmed mutation in the dystrophin gene that can be treated by skipping exon 51. EXONDYS 51 was approved under accelerated approval.

Find patient medical information for Exondys-51 intravenous on WebMD including its uses, side effects and safety, interactions, pictures, warnings and user ratings.

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