School of Pharmacy, Qingdao University, Qingdao, Shandong, China.
Phase I Clinical Research Center, The Traditional Chinese Medicine Hospital of Heze, Heze, China.
Pharmacol Res Perspect. 2021 Apr;9(2):e00729. doi: 10.1002/prp2.729.
With the improvements in relevant policies, laws, and regulations regarding drug clinical trials in China, the quantity and quality of drug clinical trials have gradually improved, and the development prospects of drug clinical trials for endocrine disorders and metabolism and nutrition disorders are promising. Based on information from the clinical trials from the online drug clinical trial registration platform of the National Medical Products Administration, we aimed to review and evaluate the development of clinical trials of drugs for endocrine disorders and metabolism and nutrition disorders in mainland China from 2010 to 2019, as well as the trends over time. A total of 861 trials were carried out on 254 types of drugs for endocrine disorders and metabolism and nutrition disorders, among which 531 (61.67%) involved endocrine disorders, and 330 (38.33%) addressed metabolism and nutrition disorders. The annual number of clinical trials has been increasing gradually, with a significant increase in 2017. Among them, the proportion of clinical trials with Chinese epidemiological characteristics was relatively large (Wu, Annual Report on Development Health Management and Health Industry in China, 2018). The largest number of trials were for diabetes drugs (55.63%), followed by trials of drugs for hyperlipidemia (19.4%) and those for hyperuricemia (7.9%). It was found that the geographical area of the leading units also showed obvious unevenness according to the analysis of the test unit data. Based on the statistics and evaluation of the data, comprehensive information is provided to support the cooperation of global pharmaceutical R&D companies and research units in China and the development of international multicenter clinical trials in China. This work additionally provides clinical trial units with a self-evaluation of scientific research competitiveness and hospital development strategies. At the same time, it provides a reference with basic data for sponsors and stakeholders in these trials to determine their development strategy goals.
随着中国药物临床试验相关政策、法规的不断完善,药物临床试验的数量和质量逐渐提高,内分泌及代谢和营养障碍领域药物临床试验的发展前景广阔。基于国家药品监督管理局药物临床试验登记与信息公示平台的临床试验信息,本文旨在回顾和评价 2010—2019 年中国大陆内分泌及代谢和营养障碍领域药物临床试验的发展,并分析其随时间的变化趋势。共开展 254 种药物的 861 项内分泌及代谢和营养障碍领域的临床试验,其中 531 项(61.67%)为内分泌疾病用药,330 项(38.33%)为代谢和营养障碍疾病用药。临床试验的年度数量逐渐增加,2017 年增幅显著。其中,具有中国流行病学特征的临床试验比例相对较大(Wu,Annual Report on Development Health Management and Health Industry in China,2018)。试验数量最多的是糖尿病药物(55.63%),其次是高血脂药物(19.4%)和高尿酸血症药物(7.9%)。根据对试验单位数据的分析,发现牵头单位的地域分布也存在明显的不均衡性。通过对数据的统计和评价,为全球制药研发企业和研究单位在中国的合作以及在中国开展国际多中心临床试验提供了综合信息支持,同时也为临床试验单位提供了科研竞争力和医院发展策略的自我评价,为这些试验的申办方和利益相关方制定发展战略目标提供了参考依据。