
US genetic medicine company Sarepta Therapeutics (Nasdaq: SRPT) has announced an update to the prescribing information for Elevidys (delandistrogene moxeparvovec-rokl), its gene therapy for Duchenne muscular dystrophy (DMD).
Safety concerns for Elevidys came to a head this summer, leading to a pause of shipments in the USA and shaving billions off the drugmaker's valuation.
Now, Sarepta reports, the product’s label will include several key updates, including a boxed warning for the risk of acute serious liver injury (ALI) and acute liver failure (ALF).
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