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Sarepta s $3 2M Gene Therapy for DMD Just Got Approved Why the Stock Is Down

Sarepta s $3 2M Gene Therapy for DMD Just Got Approved Why the Stock Is Down
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Drug administrationSarepta therapeutic

AI, Cell/Gene Therapy, Precision Medicine Drive Bullish Biotech Investment

AI, Cell/Gene Therapy, Precision Medicine Drive Bullish Biotech Investment
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US FDA approves Sarepta s gene therapy for rare muscular dystrophy in some kids

June 22 (Reuters) - The U.S. drug regulator on Thursday granted accelerated approval to Sarepta Therapeutics first-of-its-kind gene therapy for Duchenne muscular dystrophy (DMD), an inherited progressive muscle wasting disorder that almost.

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FDA approves 1st gene therapy for Duchenne muscular dystrophy

FDA approves first gene therapy for pediatric patients with Duchenne muscular dystrophy, a rare genetic condition. Elevidys is a single intravenous dose approved for patients 4 and 5 years old.

Sarepta therapeutic

FDA approval of Sarepta Duchenne genetic therapy gives me hope

If Sarepta's gene therapy SRP-9001 succeeded through this accelerated approval pathway, then many more can as well.

Drug administrationSarepta therapeuticSolid biosciences

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