Catalent’s stock $CTLT has dropped by as much as 17% to $33 on the Nasdaq after Sarepta announced on Monday that its Duchenne muscular dystrophy gene therapy did not succeed in the primary endpoint of a Phase III study.
On Jan. 5, Catalent and Sarepta announced that their collaboration was expanded so that the CDMO would produce the DMD asset for commercial use. On June 22, the gene therapy, marketed as Elevidys, received an accelerated approval from the FDA for DMD in boys aged 4 and 5.
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