FDA Official Intervenes in Sarepta Therapy Dispute, Upcoming Advisory Committee Meetings Announced

TL;DR Summary
FDA staff were leaning towards rejecting Sarepta Therapeutics' gene therapy for Duchenne muscular dystrophy, but a top official, Peter Marks, intervened and directed staff to schedule a public hearing on the therapy. Marks is a vocal advocate for faster gene therapy approvals.
Topics:business#duchenne-muscular-dystrophy#fda#gene-therapy#health#peter-marks#sarepta-therapeutics
- With FDA staff opposed to Sarepta therapy, top official intervened STAT
- Cellular, Tissue, and Gene Therapies Advisory Committee May 12, 2023 Meeting Announcement - 05/12/2023 FDA.gov
- Vaccines and Related Biological Products Advisory Committee May 18, 2023 Meeting Announcement - 05/18/2023 FDA.gov
- View Full Coverage on Google News
Reading Insights
Total Reads
0
Unique Readers
1
Time Saved
1 min
vs 1 min read
Condensed
75%
171 → 42 words
Want the full story? Read the original article
Read on STAT