FDA lifts shipping pause for Elevidys in ambulatory DMD patients
Sarepta Therapeutics (Nasdaq: SRPT) has been cleared by the American medicines regulator to resume shipments of its gene therapy Elevidys (delandistrogene moxeparvovec-rokl) for ambulatory patients with Duchenne muscular dystrophy (DMD).
The decision follows the conclusion of an investigation into the recent death of an 8-year-old patient in Brazil, which the regulator confirmed was not linked to the therapy.
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