Sarepta Therapeutics, Inc.’s gene therapy setback in Duchenne muscular dystrophy (DMD) could be Pfizer Inc.s gain. One day after Sarepta announced that the Phase III confirmatory trial testing Elevidys (delandistrogene moxeparvovec-rokl) in DMD failed to meet the primary endpoint, Pfizer said it remains hopeful that its DMD gene therapy, fordadistrogene movaparvovec, could yield stronger Phase III data.
Key Takeaways
- Pfizer's DMD gene therapy is in Phase III with interim data expected by the end of the year.
- Pfizer has deprioritized gene therapy more generally but...
“This makes our gene therapy, in a way, the main game,” worldwide president R&D Mikael Dolsten said during the company’s third quarter sales and earnings call on 31 October.