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评估药物开发过程中肾功能受损的患者:2019 年美国 FDA 药物科学和临床药理学顾问委员会会议重点。

Evaluating Patients With Impaired Renal Function During Drug Development: Highlights From the 2019 US FDA Pharmaceutical Science and Clinical Pharmacology Advisory Committee Meeting.

机构信息

Office of Clinical Pharmacology, Office of Translational Sciences, Center for Drug Evaluation and Research, US Food and Drug Administration, Silver Spring, Maryland, USA.

Theravance Biopharma US, Inc., South San Francisco, California, USA.

出版信息

Clin Pharmacol Ther. 2021 Aug;110(2):285-288. doi: 10.1002/cpt.2151. Epub 2021 Feb 16.

Abstract

Patients with multiple chronic conditions, including more advanced chronic kidney disease (CKD), are often excluded from clinical trials, creating challenges in deriving appropriate dosing information and labeling. This article summarizes the May 7, 2019, US Food and Drug Administration Pharmaceutical Science and Clinical Pharmacology Advisory Committee Meeting, which solicited expert opinions on how to enroll patients with more advanced CKD into clinical trials as well as the assumptions behind and different approaches of exposure-matching.

摘要

患有多种慢性疾病的患者,包括更晚期的慢性肾脏病(CKD),通常被排除在临床试验之外,这给获得合适的剂量信息和标签带来了挑战。本文总结了 2019 年 5 月 7 日美国食品和药物管理局药物科学和临床药理学顾问委员会会议,会议征求了专家关于如何将更晚期 CKD 患者纳入临床试验的意见,以及暴露匹配背后的假设和不同方法。

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