协变量
医学
食品药品监督管理局
随机对照试验
范围(计算机科学)
临床试验
药品
重症监护医学
梅德林
研究设计
药品管理局
替代医学
基线(sea)
临床药理学
药品审批
样本量测定
外部有效性
药物开发
药理学
临床研究设计
第N部分,共1次审判
随机化
药物试验
荟萃分析
出处
期刊:Clinical Trials
[SAGE Publishing]
日期:2025-12-31
卷期号:23 (3): 259-262
被引量:2
标识
DOI:10.1177/17407745251405770
摘要
In May 2023, the US Food and Drug Administration released a guidance document on adjusting for covariates in randomized clinical trials for drugs and biological products. This article provides a summary of motivations for the US Food and Drug Administration guidance document, recommendations in the guidance document, considerations for covariate adjustment in large trials and small trials, and additional topics beyond the scope of the guidance document that may benefit from greater consensus on best practices. A covariate-adjusted prespecified primary analysis can have advantages over an unadjusted analysis and is generally acceptable to the US Food and Drug Administration.
科研通智能强力驱动
Strongly Powered by AbleSci AI