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BRIEF-FDA accepts supplemental biologics license application for Prolia
2017年10月9日 / 晚上8点08分 / 12 天前

BRIEF-FDA accepts supplemental biologics license application for Prolia

Oct 9 (Reuters) - Amgen Inc

* FDA accepts supplemental biologics license application for Prolia® (denosumab) in glucocorticoid-induced osteoporosis

* Amgen Inc - ‍FDA has set a prescription drug user fee act (PDUFA) action date of May 28, 2018​

* Amgen Inc - ‍adverse events and serious adverse events were similar between treatment groups and consistent with known safety profile of Prolia​ Source text for Eikon: Further company coverage:

我们的标准:汤森路透“信任原则”
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