Sarepta sinks as Elevidys misses DMD endpoint in confirmator

Sarepta sinks as Elevidys misses DMD endpoint in confirmatory trial

Failing to meet the primary endpoint in its confirmatory phase III Embark trial, Sarepta Therapeutics Inc.’s gene therapy, Elevidys (delandistrogene moxeparvovec), which received accelerated approval in June and was priced at $3.2 million, has one of three fates in its future, all of which are dependent on how the U.S. FDA perceives the data.

Related Keywords

, Sarepta Therapeutics Inc , Sarepta Therapeutics , Elevidys , Delandistrogene Moxeparvovec , Duchenne Muscular Dystrophy , Admd , Embark , Phase Iii ,

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