
363: What Vinay Prasad’s ouster means for biotech and the FDA
The Readout Loud
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Navigating Post-Marketing Commitments and Drug Safety
This chapter examines the challenges of post-marketing data collection for drugs with accelerated approval, particularly a gene therapy for Duchenne muscular dystrophy. It discusses the FDA's difficulties in monitoring side effects and emphasizes the need for improved data systems to balance patient urgency with regulatory standards.
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