Another negative development for Elevidys
As if there had not been enough negative news regarding Elevidys (delandistrogene moxeparvovec) this month, there was more today from the European regulator.
The European Medicines Agency’s (EMA) human medicine commit (CHMP) issued a negative opinion on the conditional marketing authorization (CMA) for Elevidys for ambulatory individuals aged three to seven years with Duchenne muscular dystrophy (DMD).
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