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Internal FDA Fighting on Sarepta Bad Omen for Stem Cell Oversight? - The Niche
The FDA caused major controversy by approving the drug Exondys 51 from Sarepta Therapeutics for treating Duchenne muscular dystrophy over the recommendations of a scientific panel it convened that had voted 7-3 against approval. Is this contentious Sarepta approval serve as a sign of how the FDA will deal with stem cells moving forward? Will the FDA approval, which … Internal FDA Fighting on Sarepta Bad Omen for Stem Cell Oversight? Read More »
Professor Paul Knoepfler, Ph.D.