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2021-10-06

副作用太大了，恐难以获批

欧洲药品管理局或将加速评估默克的新冠口服药

格隆汇10月5日丨据彭博，欧洲药品管理局(EMA)将考虑启动针对默克新冠口服药的加速评估进程。该公司上周宣布将尽快寻求美国食品药品管理局(FDA)的紧急使用授权。

欧洲药品管理局或将加速评估默克的新冠口服药

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