SGT-003 Granted Rare Pediatric Disease, Orphan Drug and Fast Track Designations in U.S. –
– Site initiations scheduled for April; patient dosing expected to begin in Q2 2024 –
https://www.globenewswire.com/news-release/2024/04/01/2855112/0/en/Solid-Biosciences-Receives-Rare-Pediatric-Disease-Designation-from-the-FDA-for-Duchenne-Muscular-Dystrophy-Gene-Therapy-Candidate-SGT-003.html
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