FDA Gives its Nod to Procysbi; Raptor Ascends
By Marie Powers
Tuesday, April 30, 2013
The FDA put some lift under the wings of Raptor Pharmaceutical Corp., approving the orphan drug Procysbi (RP103, cysteamine bitartrate delayed-release) on its PDUFA date in the initial indication of nephropathic cystinosis (NC).
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