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FDA greenlights Italfarmaco's drug for rare muscular dystrophy
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FDA greenlights Italfarmaco's drug for rare muscular dystrophy
Mar 21, 2024 3:56 PM

March 21 (Reuters) - The U.S. FDA has approved privately

held Italfarmaco Group's drug to treat Duchenne muscular

dystrophy (DMD), an inherited muscle-wasting disorder, the

health regulator said on Thursday.

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