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Biotech Stocks Near An Inflection Point In Gene Therapy

Biotech Stocks Near An Inflection Point In Gene Therapy
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FDA Approves Gene Therapy for Rare Muscular Dystrophy

The health regulator has granted accelerated approval to Sarepta Therapeutics first-of-its-kind gene therapy for Duchenne muscular dystrophy. ....

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US FDA approves Sarepta's gene therapy for rare muscular dystrophy in some kids | WKZO | Everything Kalamazoo

By Leroy Leo and Aditya Samal (Reuters) -The U.S. Food and Drug Administration on Thursday granted accelerated approval to Sarepta Therapeutics' first. ....

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US FDA approves Sarepta's gene therapy for rare muscular dystrophy in some kids

The U.S. health regulator has 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 always affects young boys. Sarepta said on Thursday the Food and Drug Administration had approved the treatment for children aged between 4 and 5 years who can walk. It was initially seeking approval for all DMD patients who can walk. ....

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US FDA approves Sarepta's gene therapy for rare muscular dystrophy in some kids

US FDA approves Sarepta's gene therapy for rare muscular dystrophy in some kids
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