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ClinicalTrials.gov 上注册的药物相互作用临床试验报告的已发表文章中的安全性数据不一致:一项观察性研究。

Clinical trials on drug-drug interactions registered in ClinicalTrials.gov reported incongruent safety data in published articles: an observational study.

机构信息

Department of Pharmacology, University of Split School of Medicine, Split, Croatia.

Department of Public Health, University of Split School of Medicine, Split, Croatia; Department of Research in Biomedicine and Health, University of Split School of Medicine, Split, Croatia.

出版信息

J Clin Epidemiol. 2018 Dec;104:35-45. doi: 10.1016/j.jclinepi.2018.07.017. Epub 2018 Aug 3.

DOI:10.1016/j.jclinepi.2018.07.017
PMID:30081071
Abstract

OBJECTIVE

To assess safety data of trials on drug-drug interactions (DDIs) reported in ClinicalTrials.gov and published in journal articles, since DDIs are a growing concern.

STUDY DESIGN AND SETTING

In an observational study of clinical trials retrieved by the search term "drug-drug interaction(s)," we collected the information on registration and on adverse events (AEs) from ClinicalTrials.gov and corresponding publications. Trials were included if they primarily investigated DDIs, had a National Clinical Trial identifier, and were closed and completed by October 16, 2015. Publication data were extracted until March 2017.

RESULTS

Among 1,110 eligible trials, most were in phase 1 (76.8%), industry-funded (68.8%), and started before registration (56.9%). Results were not reported in the registry for 86.8% and not published for 68.1% trials. Published AE data were completely identical to the data submitted to ClinicalTrials.gov for only 15.6% trials. Among 64 trials with results reported both in ClinicalTrials.gov and publications, 34.4% published concordant number for other AEs.

CONCLUSION

Discrepancies that emerge from incomplete or changed reporting of AEs in publications emphasize the need to amend and enforce regulatory requirements for timely and complete submission of results, clearer AE reporting for trials focusing on DDIs, and regular assessment of the congruence of AE data submitted to ClinicalTrials.gov and scientific journals during the publication process.

摘要

目的

评估 ClinicalTrials.gov 报告的药物相互作用(DDI)试验的安全性数据和已发表的期刊文章,因为 DDI 是一个日益受到关注的问题。

研究设计和设置

在一项以“药物相互作用”为检索词的临床试验观察性研究中,我们从 ClinicalTrials.gov 收集了注册和不良事件(AE)信息,并从相应的出版物中收集了信息。如果试验主要研究 DDI、具有国家临床试验标识符、并于 2015 年 10 月 16 日之前关闭和完成,则纳入研究。直到 2017 年 3 月才提取出版物数据。

结果

在 1110 项合格试验中,大多数处于 1 期(76.8%)、由工业界资助(68.8%)且在注册之前开始(56.9%)。86.8%的试验未在注册处报告结果,68.1%的试验未发表。只有 15.6%的试验发表的 AE 数据与提交给 ClinicalTrials.gov 的数据完全相同。在 64 项在 ClinicalTrials.gov 和出版物中都报告了结果的试验中,34.4%的试验对其他 AE 发表了一致的数字。

结论

由于在出版物中对 AE 的不完全或更改报告而出现的差异,强调需要修正和加强对及时和完整提交结果的监管要求,对关注 DDI 的试验更明确地报告 AE,并在出版物过程中定期评估向 ClinicalTrials.gov 和科学期刊提交的 AE 数据的一致性。

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