Sarepta’s DMD Gene Therapy: FDA Says Concluding Effectiveness Or Ineffectiveness Is ‘Challenging’

Concerns about the clinical trials, the manufacturing, and the preclusive nature of Sarepta's gene therapy for Duchenne muscular dystrophy raise questions ahead of the upcoming US FDA advisory committee meeting.

Gene therapy
The FDA said that Sarepta's commercial manufacturing process was not comparable to the process used to make SRP-9001 for early clinical studies. • Source: Shutterstock

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