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FDA Approves First Gene Therapy to Treat Duchenne Muscular Dystrophy

FRIDAY, June 23, 2023 (HealthDay News) The U.S. Food and Drug Administration on Thursday approved the drug Elevidys (delandistrogene moxeparvovec-rokl), the first gene therapy for the treatment of children

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FDA Approves First Gene Therapy for Duchenne Muscular Dystrophy

Sarepta Therapeutics’ Elevidys is now the first FDA-approved gene therapy for Duchenne muscular dystrophy. Elevidys is an engineered version of a gene intended to restore function lost to the mutation at the root of the inherited muscle disease.

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FDA grants accelerated approval to Sarepta s Duchenne muscular dystrophy gene therapy

FDA grants accelerated approval to Sarepta s Duchenne muscular dystrophy gene therapy
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Sarepta prices Duchenne gene therapy at $3 2M

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FDA Approves First Gene Therapy to Treat Duchenne Muscular Dystrophy

FRIDAY, June 23, 2023 (HealthDay News) The U.S. Food and Drug Administration on Thursday approved the drug Elevidys, the first gene therapy for the treatment of children with Duchenne

United statesPeter marksDoug ingramDrug administration onAssociated pressDrugmaker sarepta therapeutics incHealthday newsDrug administrationDrugmaker sarepta therapeuticsBiologics evaluationPat furlongParent project muscular

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