Center for Biologics Evaluation and Research, Bethesda, MD 20892, USA.
Vet Pathol. 2010 Sep;47(5):774-8. doi: 10.1177/0300985810372506. Epub 2010 Jun 15.
In 2002, the US Food and Drug Administration issued regulations to allow the approval of human drugs and biological products based on animal efficacy studies when human efficacy studies would be unethical or not feasible. These regulations are intended to assist in the approval process for products aimed at preventing or treating human diseases caused by nuclear, radiological, biological, and chemical agents that have the potential to harm a significant percentage of the US population. This article discusses the criteria that must be met to use the Animal Rule to demonstrate efficacy in place of human clinical trials.
2002 年,美国食品和药物管理局发布了规定,允许在人体功效研究不道德或不可行的情况下,根据动物功效研究批准人类药物和生物制品。这些规定旨在协助批准旨在预防或治疗由核、辐射、生物和化学制剂引起的、有可能对美国相当大一部分人口造成伤害的人类疾病的产品。本文讨论了为了用动物规则来证明功效以替代人体临床试验,必须满足的标准。