Trends in drug-drug interactions for new drug clinical trials in China over the past 10 years (2013-2022).

IF 2.7 3区 医学 Q2 PHARMACOLOGY & PHARMACY BMC Pharmacology & Toxicology Pub Date : 2025-03-21 DOI:10.1186/s40360-025-00905-3
Jianxiong Zhang, Jingxuan Wu, Jiangshuo Li, Meixia Liu, Shaodan Liu, Ruirui He, Ruihua Dong
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Abstract

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.

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近10年中国新药临床试验药物相互作用趋势(2013-2022)
近年来,中国药物相互作用(DDI)临床试验数量迅速增加。本研究的目的是总结和分析过去10年在中国进行的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网站披露的所有相关报名信息进行汇总分析。虽然2017年之前进行的DDI临床试验数量相对较少,但2017年之后明显增加。2013 - 2019年DDI临床试验平均持续时间为85.83±100.99 d, 2020 - 2022年平均持续时间为107.16±98.57 d。使用利福平的时间为5-19天,在使用利福平的5-14天后给药。伊曲康唑给药4 ~ 17 d,伊曲康唑给药3 ~ 10 d后给药。由于新药的开发和药品注册和销售政策的更新,药物相互作用的临床试验最近有所增加。尽管临床试验的设计符合新的指导方针,但相互作用药物的施用时间仍然差别很大。优化方案设计可以缩短临床试验的实施周期,降低药品营销成本。
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来源期刊
BMC Pharmacology & Toxicology
BMC Pharmacology & Toxicology PHARMACOLOGY & PHARMACYTOXICOLOGY&nb-TOXICOLOGY
CiteScore
4.80
自引率
0.00%
发文量
87
审稿时长
12 weeks
期刊介绍: BMC Pharmacology and Toxicology is an open access, peer-reviewed journal that considers articles on all aspects of chemically defined therapeutic and toxic agents. The journal welcomes submissions from all fields of experimental and clinical pharmacology including clinical trials and toxicology.
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