Department of Epidemiology and Data Science, Amsterdam UMC, University of Amsterdam, Amsterdam, The Netherlands.
School of Medicine, Imperial College London, London, UK.
Clin Trials. 2022 Apr;19(2):217-223. doi: 10.1177/17407745211071015. Epub 2022 Feb 16.
January 2019, the House of Commons' Science and Technology Committee sent letters to UK universities admonishing them to achieve compliance with results reporting requirements for Clinical Trials of Investigative Medicinal Products by summer 2019. This study documents changes in the clinical trial policies and Clinical Trials of Investigative Medicinal Product reporting performance of 20 major UK universities following that intervention.
Freedom of Information requests were filed in June 2018 and June 2020 to obtain clinical trial registration and reporting policies covering both Clinical Trials of Investigative Medicinal Products and all other clinical trials. Two independent reviewers assessed policies against transparency benchmarks based on World Health Organization best practices. To evaluate universities' trial reporting performance, we used a public online tracking tool, the European Union Trials Tracker, which assesses universities' compliance with regulatory Clinical Trials of Investigative Medicinal Product disclosure requirements on the European Clinical Trial Register. Specifically, we evaluated whether universities were adhering to the European Union requirement to post summary results on the trial registry within 12 months of completion.
Mean policy strength increased from 2.8 to 4.9 points (out of a maximum of 7 points) between June 2018 and June 2020. In October 2018 the average percentage of due Clinical Trials of Investigative Medicinal Products that had results available on the European trial registry across university sponsors included in the cohort was 29%. By June 2021, this had increased to 91%, with 5 universities achieving a reporting performance of 100%. All 20 universities reported more than 70% of their due trial results on the European trial registry.
Political pressure appears to have a significant positive impact on UK universities' clinical trial reporting policies and performance. Similar approaches could be used to improve reporting performance for other types of sponsors, other types of trials, and in other countries.
2019 年 1 月,英国下议院科学技术委员会向英国各大学发出信函,谴责它们未能遵守 2019 年夏季之前提交临床试验结果的规定。本研究记录了在这一干预措施之后,20 所英国主要大学的临床试验政策和调查性药品临床试验报告绩效的变化。
2018 年 6 月和 2020 年 6 月,我们根据信息自由请求,获取涵盖调查性药品临床试验和所有其他临床试验的临床试验注册和报告政策。两名独立的审查员根据世界卫生组织最佳实践的透明度基准评估政策。为了评估大学的试验报告绩效,我们使用了一个公共在线跟踪工具,即欧盟试验跟踪器,该工具评估大学在欧洲临床试验注册中心遵守监管调查性药品临床试验披露要求的情况。具体而言,我们评估了大学是否遵守了在试验完成后 12 个月内在试验登记处公布试验总结结果的欧盟要求。
2018 年 6 月至 2020 年 6 月期间,政策力度平均从 2.8 分提高到 4.9 分(满分 7 分)。2018 年 10 月,在纳入队列的大学赞助商中,有结果可在欧洲试验登记处获得的应报告调查性药品临床试验的平均百分比为 29%。到 2021 年 6 月,这一比例增加到 91%,其中 5 所大学的报告绩效达到 100%。所有 20 所大学都在欧洲试验登记处报告了超过 70%的应报告试验结果。
政治压力似乎对英国大学的临床试验报告政策和绩效产生了重大积极影响。类似的方法可用于提高其他类型赞助商、其他类型试验和其他国家的报告绩效。