FDA: Prasugrel [Regulatives / Guidelines]

posted by intuitivepharma – India, 2013-12-20 08:36 (4576 d 13:33 ago) – Posting: # 12084
Views: 31,914

Dear Helmut,

How about this bioequivalence requirement [based on USFDA individual product bioequivalence recommendations] for Prasugrel Hydrochloride

Active ingredient: Prasugrel Hydrochloride

Analytes to measure (in appropriate biological fluid): Inactive metabolite R-95913 and active metabolite R-138727 in plasma.

Bioequivalence based on (90% CI): Inactive metabolite R-95913.

Please submit the data of active metabolite (R-138727) including individual and mean concentrations, individual and mean pharmacokinetic parameters, and geometric means and ratios of means for AUC and Cmax, as supportive evidence of comparable therapeutic outcome.

Can I justify my ANDA if test formulation is bioequivalent for the active metabolite (R-138727) and not bioequivalent for the Inactive metabolite R-95913? :confused:


Edit: Subject line changed. [Helmut]

Thanks & Regards,
IP.

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