Wednesday, September 24, 2008

PPD Confirms Takeda's NDA Submission of Alogliptin and Actos to U.S. Food and Drug Administration

PPD, Inc. (Nasdaq: PPDI) today confirmed that Takeda Pharmaceutical Company Limited has submitted a new drug application to the U.S. Food and Drug Administration for marketing approval of alogliptin (SYR-322) and ACTOS(R) (pioglitazone HCl) in a single tablet for the treatment of type 2 diabetes.

The details can be read here.

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