FDA to review Sarepta's Duchenne gene therapy for traditional approval

FDA to review Sarepta's Duchenne gene therapy for traditional approval

Source: 
Reuters
snippet: 

Sarepta Therapeutics (SRPT.O) said on Friday that the US FDA would review an application seeking traditional approval for its gene therapy to treat a muscle-wasting disorder by June 21, months after it failed the main goal of a confirmatory trial.