Prognosis
FDA Moving at ‘Lightning Speed’ on Gilead Drug, Commissioner Says
- Commissioner Hahn says agency wants to see totality of data
- Several different pathways available for review, Hahn says
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The Food and Drug Administration is moving at “lightning speed” to review data on Gilead Sciences Inc.’s experimental Covid-19 treatment remdesivir, Commissioner Stephen Hahn said, after encouraging results emerged from a key U.S. trial.