临床试验
医学
随机对照试验
抗癌药
药品
临床研究设计
药理学
临床研究
适应性设计
肿瘤科
内科学
作者
Xingxian Luo,Qixiang Guo,Xin Du,Lin Huang,Shein‐Chung Chow,Yang Yue
标识
DOI:10.1016/j.drudis.2023.103578
摘要
China has greatly facilitated the approval of many novel anticancer drugs since the drug regulatory reform in 2015. Here, we review the clinical trial designs used in pivotal clinical trials for approved anticancer agents in China from 2015 to 2021. Overall, 79 new molecular entities (NMEs) with 140 anticancer indications were identified. Of these, adaptive randomized controlled trial (RCT) designs were used most frequently in pivotal clinical trials (n = 83, 49%), followed by single-arm design trials (n = 52, 30%) and traditional RCT design trials (n = 36, 21%). The single-arm trials and adaptive RCTs can significantly shorten clinical trial duration compared with traditional RCT designs. Our findings showed that novel clinical trial designs were widely used in China to accelerate the launch of anticancer drugs.
科研通智能强力驱动
Strongly Powered by AbleSci AI