Monday, 27 October 2014

FDA seeks more data on Sarepta muscle disorder drug, shares slump


The headquarters of the U.S. Food and Drug Administration is shown in Silver Spring near Washington By Natalie Grover (Reuters) - Sarepta Therapeutics Inc suffered yet another setback after U.S. regulators asked for more data on its experimental muscle disorder drug, a move that further delays the marketing application for the treatment. Nearly a third of Sarepta's market value was wiped out on Monday after the company disclosed the U.S. Food and Drug Administration's decision on eteplirsen, its lead drug. ...








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