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Bristol-Myers Squibb Company (NYSE: BMY) and AstraZeneca (NYSE: AZN) announced that their marketing authorization application for ONGLYZA™ (saxagliptin) received a positive opinion from the Committee for Medicinal Products for Human Use (CHMP) for the treatment of type 2 diabetes in adults as add-on therapy with metformin, a thiazolidinedione or a sulphonylurea.
BAGSVAERD, DENMARK--(Marketwire - July 3, 2009) - Novo Nordisk's Victoza® (liraglutide) receives marketing authorisation in Europe Novo Nordisk announced today that the European Commission has granted marketing authorisation for Victoza® for the treatment of type 2 diabetes in adults. The authorisation covers all 27 European Union member states. Victoza® is the brand name approved in Europe for ...
OSAKA, Japan, June 29, 2009 – Takeda Pharmaceutical Company Limited (Takeda) today announced that it submitted an application for an additional indication of alogliptin (generic name, development code: SYR-322) for combination therapy with thiazolidinediones, and a new drug application (NDA) of fixed-dose combination (FDC) of alogliptin and pioglitazone HCl (generic name, tradename in Japan: ...
Takeda Pharmaceutical Company Limited (Takeda) announced that it submitted an application for an additional indication of alogliptin (generic name, development code: SYR-322) for combination therapy with thiazolidinediones, and a new drug application (NDA) of fixed-dose combination (FDC) of alogliptin and pioglitazone HCl (generic name, tradename in Japan: Actos) to the Ministry of Health, ...
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