Suppr超能文献

关于临床试验数据透明度与披露的观点。

Perspectives on clinical trial data transparency and disclosure.

作者信息

Alemayehu Demissie, Anziano Richard J, Levenstein Marcia

机构信息

Pfizer Inc., United States.

Pfizer Inc., United States.

出版信息

Contemp Clin Trials. 2014 Sep;39(1):28-33. doi: 10.1016/j.cct.2014.07.002. Epub 2014 Jul 11.

Abstract

The increased demand for transparency and disclosure of data from clinical trials sponsored by pharmaceutical companies poses considerable challenges and opportunities from a statistical perspective. A central issue is the need to protect patient privacy and adhere to Good Clinical and Statistical Practices, while ensuring access to patient-level data from clinical trials to the wider research community. This paper offers options to navigate this dilemma and balance competing priorities, with emphasis on the role of good clinical and statistical practices as proven safeguards for scientific integrity, the importance of adopting best practices for reporting of data from secondary analyses, and the need for optimal collaboration among stakeholders to facilitate data sharing.

摘要

制药公司赞助的临床试验对数据透明度和披露的需求增加,从统计学角度来看带来了相当大的挑战和机遇。一个核心问题是,在确保更广泛的研究界能够获取临床试验患者层面数据的同时,需要保护患者隐私并遵守良好临床和统计规范。本文提供了应对这一困境并平衡相互竞争的优先事项的选项,重点强调良好临床和统计规范作为科学诚信的可靠保障的作用、采用二次分析数据报告最佳实践的重要性,以及利益相关者之间进行最佳协作以促进数据共享的必要性。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验