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证据揭示研究:探索欧洲制药行业如何利用真实世界证据和复杂临床试验设计。

The Evidence REVEAL Study: Exploring the Use of Real-World Evidence and Complex Clinical Trial Design by the European Pharmaceutical Industry.

机构信息

Technopolis Group, Brighton, UK.

Technopolis Group, Amsterdam, the Netherlands.

出版信息

Clin Pharmacol Ther. 2021 Nov;110(5):1180-1189. doi: 10.1002/cpt.2103. Epub 2020 Dec 17.

Abstract

The rapid evolution of science and technology allows innovative approaches to generate new types of evidence about the effectiveness of medical product development so as to speed up patients' access to better diagnostics and treatment. Our study explored how two emerging approaches, the use of real-world evidence (RWE) and complex clinical trial (CCT) design, are currently being used by the pharmaceutical industry to support premarketing authorization of medical product development and reviewed the international landscape for regulatory acceptance of such novel approaches. Combining evidence from a literature review, company survey, and interviews with international regulators and experts, we found that 80% of Europe-based pharmaceutical companies have used RWE and 50% have used CCTs, in some capacity. Further, we present case examples of how companies are using these approaches and how international regulators are preparing for such developments. To conclude, we provide a set of recommendations for European industry and regulators to consider so that these novel approaches achieve their full potential within the EU regulatory system.

摘要

科学技术的迅速发展使得人们能够采用创新方法来生成有关医疗产品开发效果的新型证据,从而加快患者获得更好的诊断和治疗的速度。我们的研究探讨了制药行业目前如何利用两种新兴方法(真实世界证据(RWE)和复杂临床试验(CCT)设计)来支持医疗产品开发的上市前授权,并审查了此类新方法在国际监管接受方面的情况。我们结合文献综述、公司调查以及与国际监管机构和专家的访谈证据,发现 80%的欧洲制药公司在某种程度上使用了 RWE,50%的公司使用了 CCT。此外,我们还介绍了一些公司如何使用这些方法的案例,以及国际监管机构为此类发展做了哪些准备。最后,我们为欧洲企业和监管机构提供了一系列建议,以便这些新方法在欧盟监管体系中充分发挥潜力。

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