20
May

The FDA has given Sarepta Therapeutics the go-ahead to start a rolling submission for its Duchenne muscular dystrophy drug, eteplirsen. The green light comes 7 weeks after Sarepta parted company with its CEO Chris Garabedian–and his interim successor was quick to frame the regulatory breakthrough as the result of the subsequent shift in strategy.

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Source: Sarepta surges after kicking off a rolling submission for its DMD drug

    

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