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BioWorld - Saturday, December 13, 2025
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» FDA Gives its Nod to Procysbi; Raptor Ascends
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FDA Gives its Nod to Procysbi; Raptor Ascends
May 1, 2013
By
Marie Powers
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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