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美国药品评价和研究中心(CDER)动物实验3R原则的实施:过去、现在与未来

Implementation of the principles of the 3Rs of animal testing at CDER: Past, present and future.

作者信息

Wange Ronald L, Brown Paul C, Davis-Bruno Karen L

机构信息

US Food and Drug Administration, Center for Drug Evaluation and Research, Silver Spring, MD, USA.

US Food and Drug Administration, Center for Drug Evaluation and Research, Silver Spring, MD, USA.

出版信息

Regul Toxicol Pharmacol. 2021 Jul;123:104953. doi: 10.1016/j.yrtph.2021.104953. Epub 2021 May 11.

Abstract

The safety testing of pharmaceutical candidates has traditionally relied on data gathered from studies in animals, and these sources of information remain a vital component of the safety assessment for new drug and biologic products. However, there are clearly ethical implications that attend the use of animals for safety testing, and FDA fully supports the principles of the 3Rs, as it relates to animal usage; these being to replace, reduce and refine. We provide an overview of some of the events and activities (legal and programmatic) that have had, and continue to have, the greatest impact on animal use in pharmaceutical development, and highlight some ongoing efforts to further meet the challenge of achieving our mission as humanely as possible.

摘要

传统上,候选药物的安全性测试依赖于从动物研究中收集的数据,这些信息来源仍然是新药和生物制品安全性评估的重要组成部分。然而,使用动物进行安全性测试显然存在伦理问题,美国食品药品监督管理局(FDA)全力支持与动物使用相关的3R原则,即替代、减少和优化。我们概述了一些对药物研发中动物使用产生了并将继续产生最大影响的事件和活动(法律和计划方面的),并强调了为进一步应对尽可能人道地实现我们使命的挑战而正在进行的一些努力。

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