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BRIEF-Pfizer says U.S. FDA and EMA accept regulatory submissions for bosuliffor
2017年8月29日 / 上午11点19分 / 3 个月前

BRIEF-Pfizer says U.S. FDA and EMA accept regulatory submissions for bosuliffor

Aug 29 (Reuters) - Pfizer Inc

* U.S. FDA and European Medicines Agency accept regulatory submissions for Bosulif® (bosutinib) for the treatment of patients with newly diagnosed Ph+ chronic myeloid leukemia

* Says ‍prescription drug user fee act (PDUFA) goal date for a decision by FDA is in December 2017​ Source text for Eikon: Further company coverage:

我们的标准:汤森路透“信任原则”
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