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在创新性确证性临床试验中利用历史受试者水平数据减轻患者负担:方法与机遇综述

Minimizing Patient Burden Through the Use of Historical Subject-Level Data in Innovative Confirmatory Clinical Trials: Review of Methods and Opportunities.

作者信息

Lim Jessica, Walley Rosalind, Yuan Jiacheng, Liu Jeen, Dabral Abhishek, Best Nicky, Grieve Andrew, Hampson Lisa, Wolfram Josephine, Woodward Phil, Yong Florence, Zhang Xiang, Bowen Ed

机构信息

1 Clinical Statistics, GlaxoSmithKline, Collegeville, PA, USA.

2 Centre for Excellence in Statistical Innovation, UCB, UK.

出版信息

Ther Innov Regul Sci. 2018 Sep;52(5):546-559. doi: 10.1177/2168479018778282. Epub 2018 Jun 18.

Abstract

The goal of clinical trial research is to deliver safe and efficacious new treatments to patients in need in a timely and cost-effective manner. There is precedent in using historical control data to reduce the number of concurrent control subjects required in developing medicines for rare diseases and other areas of unmet need. The purpose of this paper is to provide a review for a regulatory and industry audience of the current state of relevant statistical methods, and of the uptake of these approaches and the opportunities for broader use of historical data in confirmatory clinical trials. General principles to consider when incorporating historical control data in a new trial are presented. Bayesian and frequentist approaches are outlined including how the operating characteristics for such a trial can be obtained. Finally, examples of approved new treatments that incorporated historical controls in their confirmatory trials are presented.

摘要

临床试验研究的目标是以及时且具有成本效益的方式,为有需要的患者提供安全有效的新疗法。在为罕见病及其他未满足需求领域开发药物时,利用历史对照数据来减少所需同期对照受试者数量已有先例。本文旨在为监管机构和行业受众综述相关统计方法的现状、这些方法的采用情况以及在确证性临床试验中更广泛使用历史数据的机会。文中介绍了在新试验中纳入历史对照数据时应考虑的一般原则。概述了贝叶斯方法和频率论方法,包括如何获得此类试验的操作特征。最后,列举了在确证性试验中纳入历史对照的获批新疗法实例。

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