Sarepta Therapeutics Inc.’s plans to get its drug Exondys 51 (eteplirsen) approved in Europe this year have been derailed by regulatory advisors there, but the Boston, Mass.-based biotech's CEO has vowed to do what it takes to get the proposed treatment for Duchenne muscular dystrophy (DMD) re-assessed - and ultimately launched - on the European market.
Sarepta used its first-quarter earnings update on May 3 to announce that it received a negative trend vote following its...








