Evaluation of clinical trial designs for novel anticancer drugs in China: A cohort study of drugs approved between 2015 and 2021

被引:2
|
作者
Luo, Xingxian [1 ,2 ,3 ]
Guo, Qixiang [1 ,2 ]
Du, Xin [1 ,2 ]
Huang, Lin [5 ]
Chow, Shein-Chung [4 ]
Yang, Yue [1 ,2 ]
机构
[1] Tsinghua Univ, Sch Pharmaceut Sci, Beijing, Peoples R China
[2] Natl Med Prod Adm, Key Lab Innovat Drug Res & Evaluat, Beijing, Peoples R China
[3] Tsinghua Peking Ctr Life Sci, Beijing, Peoples R China
[4] Duke Univ, Biostat & Bioinformat, Sch Med, Durham, NC 27708 USA
[5] Peking Univ Peoples Hosp, Dept Pharm, Beijing, Peoples R China
关键词
anticancer drugs; single-arm design; adaptive design; randomized controlled trial; China; EXPERIENCE; HISTORY;
D O I
10.1016/j.drudis.2023.103578
中图分类号
R9 [药学];
学科分类号
1007 ;
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.
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页数:6
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