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ACTUALITES

Takeda Provides Update on EU Marketing Authorization Application for NINLARO® ...


- 28 Mai 2016 modifié le 1 Janvier 1970


(BUSINESS WIRE)-- Takeda Pharmaceutical Company Limited (TSE: 4502) today announced that the European Medicines Agency's (EMA) Committee for Medicinal Products for Human Use (CHMP) has adopted a negative opinion, recommending against the authorization of NINLARO® (ixazomib) capsules, an oral proteasome inhibitor for the treatment of patients with relapsed and/or refractory multiple myeloma. Takeda intends to appeal this opinion and request a re-examination by the CHMP.

“We are disappointed by the CHMP's opinion. ...

Source : http://me-newswire.net//news/18021/en...



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