Eli Lilly and Co., Indianapolis, IN 46225, USA.
Int J Toxicol. 2011 Oct;30(5):583-90. doi: 10.1177/1091581811415875.
Selection of a pharmacologically responsive species can represent a major challenge in designing nonclinical safety assessment programs for many biopharmaceuticals (eg, monoclonal antibodies (mAbs)). Frequently, the only relevant species for nonclinical testing of mAbs is the non-human primate (NHP). This situation, coupled with a rapidly increasing number of mAb drugs in development, has resulted in a significant increase in the number of NHPs used in nonclinical safety assessment. Apart from ethical considerations related to responsible animal use, there is a clear need for more efficient and innovative approaches to drug discovery and development; these factors drive the need to investigate alternative approaches and strategies for the safety assessment. This review summarizes important scientific and regulatory perspectives derived from presentations and audience discussions in an educational forum at the 2010 annual American College of Toxicology meeting regarding opportunities for employing alternative approaches to minimize NHP use in mAb drug development.
在设计许多生物制药(例如单克隆抗体(mAbs))的非临床安全性评估方案时,选择一种药理反应敏感的物种可能是一项重大挑战。通常,mAbs 非临床测试的唯一相关物种是非人灵长类动物(NHP)。这种情况,再加上越来越多的 mAb 药物正在开发中,导致用于非临床安全性评估的 NHPs 数量显著增加。除了与负责任地使用动物相关的伦理考虑外,显然还需要更有效和创新的方法来进行药物发现和开发;这些因素促使人们需要研究替代方法和策略来进行安全性评估。本综述总结了在 2010 年美国毒理学会年会上的一个教育论坛的演讲和观众讨论中得出的重要科学和监管观点,这些观点涉及在 mAb 药物开发中采用替代方法来最小化 NHP 使用的机会。