FDA greenlights Italfarmaco's drug for rare muscular dystrophy

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.

(Reporting by Sruthi Narasimha Chari and Mariam Sunny in Bengaluru; Editing by Krishna Chandra Eluri)

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