Sistare F D, DeGeorge J J
Safety Assessment, Merck and Co. Inc., West Point, Pennsylvania, USA.
Clin Pharmacol Ther. 2007 Aug;82(2):210-4. doi: 10.1038/sj.clpt.6100243. Epub 2007 May 16.
Toxicology studies in animals are required by regulatory authorities worldwide to provide assurances that clinical testing of pharmaceutical candidates can be conducted safely. Safety concerns from animal studies account for over 20% of attritions from drug development. As discordance between humans and animals is expected, two goals of safe and efficient drug development must be (1) to improve the human relevance of animal testing with new models and technologies, and (2) to advance quickly to clinical testing armed with improved safety biomarker tools.
全球监管机构要求开展动物毒理学研究,以确保药物候选物的临床试验能够安全进行。动物研究引发的安全问题占药物研发淘汰率的20%以上。由于预计人与动物之间存在差异,安全高效药物研发的两个目标必须是:(1)利用新模型和技术提高动物试验与人类的相关性;(2)借助改进的安全生物标志物工具迅速推进到临床试验阶段。