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Takeda Files DPP-4 Inhibitor NDA, Poised To Best Bristol/AstraZeneca, Novartis In Race For Second To Market

This article was originally published in PharmAsia News

Executive Summary

Takeda submitted an NDA for its dipeptidyl peptidase-4 inhibitor alogliptin (SYR-322) for type 2 diabetes Dec. 27, potentially positioning the Japanese pharma to be second to market with a drug in the class

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TOKYO - Takeda Pharmaceutical said Sept. 24 its U.S. R&D subsidiary, Takeda Global Research & Development Center, had applied to the U.S. Food and Drug Administration for approval to market an alogliptin/Actos combination tablet for the treatment of type 2 diabetes

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