Marathon Pharmaceuticals' DMD drug deflazacort granted FDA Priority Review status

11 August 2016

The US Food and Drug Administration (FDA) has granted Priority Review status to privately-held Marathon Pharmaceuticals’ investigational drug deflazacort for Duchenne muscular dystrophy (DMD).

New Drug Applications (NDA) for immediate-release tablet formulations and for an oral suspension formulation were also accepted for review by the FDA.

Priority Review status is reserved for drugs that offer significant improvements over existing options or provide a treatment for a condition for which no approved treatment currently exists.

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