Changes in Early-Phase Clinical Trials in China During 2013–2022: A Review

Jianxiong Zhang, Peng Zhang, Haixue Wang, Ruihua Dong
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Abstract

Clinical trials on innovative drugs in China have witnessed a stage of rapid development in recent years. The introduction of a number of government policies has stimulated enthusiasm for research and development in the pharmaceutical industry. We analyzed the data of the early-phase 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, including posted time, drug classification, dosing formula, indications, trial design, and trial status, were summarized and analyzed. A total of 5336 early-phase clinical trials were identified. The quantity and growth rate of early-phase clinical trials have increased substantially each year. Chemical drugs accounted for the largest proportion of early-phase clinical trials, although it dropped from 85.7% in 2013 to 59.5% in 2022. Moreover, the number of oncology drugs has increased yearly, accounting for 49.2% of all early-phase clinical trials in 2022. We can conclude that during 2013–2022, the development of early-phase clinical trials has progressed due to government support and advanced development techniques. To enhance the efficiency and success rate of early-phase clinical trials in the future, it is necessary to acquire advanced technical support and improve standardized supervision systems.

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2013-2022年中国早期临床试验的变化:综述
近年来,中国的创新药物临床试验进入了快速发展阶段。政府多项政策的出台激发了医药行业的研发热情。我们分析了 2013 年 9 月 6 日至 2022 年 12 月 31 日在中国药品审评中心(CDE)注册的早期临床试验数据。我们汇总并分析了 CDE 网站上披露的所有相关注册信息,包括公布时间、药物分类、剂量配方、适应症、试验设计和试验状态等。共发现 5336 项早期临床试验。早期临床试验的数量和增长率逐年大幅增长。化学药物在早期临床试验中所占比例最大,但已从2013年的85.7%降至2022年的59.5%。此外,肿瘤药物的数量也在逐年增加,2022 年将占所有早期临床试验的 49.2%。由此可见,2013-2022 年间,由于政府的支持和先进的研发技术,早期临床试验的发展取得了长足的进步。未来,要提高早期临床试验的效率和成功率,必须获得先进的技术支持,完善规范的监管体系。
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