食品药品监督管理局
授权
药品审批
临床试验
医学
药品
重症监护医学
销售授权
药理学
生物信息学
内科学
生物
计算机安全
计算机科学
作者
Xuezhou Mao,G. Caleb Alexander,Guanqiao Li
标识
DOI:10.1016/j.ccell.2024.09.005
摘要
We compare the clinical trial success rates of products receiving US Food and Drug Administration (FDA) accelerated approval (AA) to those approved without using this pathway. Our findings raise important questions about how the AA pathway can best optimize early access to therapeutics that are ultimately proven safe and effective.
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