Zhang Jianxiong, Wu Jingxuan, Li Jiangshuo, Liu Meixia, Liu Shaodan, He Ruirui, Dong Ruihua
Research Ward, Beijing Friendship Hospital, Capital Medical University, No. 95 Yong An Road, Xicheng District, Beijing, 100050, China.
Beijing Key Laboratory of Early Clinical Evaluation of Nucleic Acid Products and Cell Therapy, Beijing, China.
BMC Pharmacol Toxicol. 2025 Mar 21;26(1):66. doi: 10.1186/s40360-025-00905-3.
The number of drug-drug interaction (DDI) clinical trials in China has increased rapidly in recent years. The aim of this study was to summarize and analyze DDI clinical trials in China over the past 10 years. We conducted a cross-sectional study of DDI clinical trials registered in the Chinese Center for Drug Evaluation (CDE) from September 6, 2013 to December 31, 2022. All related registration information disclosed on the CDE website were summarized and analyzed. Although the number of DDI clinical trials conducted before 2017 was relatively low, it increased markedly after 2017. The average duration of DDI clinical trials was 85.83 ± 100.99 days from 2013 to 2019 and 107.16 ± 98.57 days from 2020 to 2022. The duration of rifampicin use was 5-19 days, and the investigational drug was administered after 5-14 days of rifampicin use. Itraconazole was administered for 4-17 days, and the investigational drug was administered after 3-10 days of itraconazole use. Clinical trials of drug-drug interactions have recently increased due to the development of new drugs and the updated policies regulating drug registration and marketing. Although the designs of clinical trials comply with the new guidelines, the duration of the administration of interacting drugs still varies widely. Optimizing protocol designs can shorten the implementation period of clinical trials and reduce the costs of drug marketing.
近年来,中国药物相互作用(DDI)临床试验的数量迅速增加。本研究的目的是总结和分析中国过去10年的DDI临床试验。我们对2013年9月6日至2022年12月31日在中国国家药品监督管理局药品审评中心(CDE)注册的DDI临床试验进行了横断面研究。对CDE网站上披露的所有相关注册信息进行了总结和分析。尽管2017年之前进行的DDI临床试验数量相对较少,但2017年之后显著增加。2013年至2019年DDI临床试验的平均持续时间为85.83±100.99天,2020年至2022年为107.16±98.57天。利福平的使用时间为5 - 19天,在利福平使用5 - 14天后给予试验药物。伊曲康唑给药4 - 17天,在伊曲康唑使用3 - 10天后给予试验药物。由于新药的开发以及药物注册和上市监管政策的更新,药物相互作用的临床试验最近有所增加。尽管临床试验设计符合新指南,但相互作用药物的给药持续时间仍差异很大。优化方案设计可以缩短临床试验的实施周期并降低药物上市成本。