Department of Pharmacokinetic and Pharmacodynamic Sciences, Genentech, Inc., 1 DNA Way, Mail Stop 463A, South San Francisco, California 94080, USA.
Expert Opin Drug Metab Toxicol. 2012 Feb;8(2):141-60. doi: 10.1517/17425255.2012.643868. Epub 2012 Jan 17.
The number of monoclonal antibodies available for clinical use and under development has dramatically increased in the last 10 years. Understanding their pharmacokinetics and pharmacodynamics is essential for selecting the right clinical candidate, correct dose and regimen for a target indication.
This article reviews the existing literature and knowledge of monoclonal antibodies. Specifically, the authors discuss monoclonal antibodies with respect to their pharmacokinetics (including absorption, distribution and elimination) and their pharmacodynamics. The authors also look at the pharmacokinetic/pharmacodynamic relationship, scaling from preclinical to clinical studies and selection of the first-in-human dose.
Monoclonal antibodies have complex pharmacokinetic and pharmacodynamic characteristics that are dependent on several factors. Therefore, it is important to improve our understanding of the pharmacokinetics and pharmacodynamics of monoclonal antibodies from a basic research standpoint. It is also equally important to apply mechanistic pharmacokinetic/pharmacodynamic models to interpret the experimental results and facilitate efforts to predict the safety and efficacy of monoclonal antibodies.
在过去的 10 年中,可用于临床使用和正在开发的单克隆抗体的数量急剧增加。了解它们的药代动力学和药效学对于选择合适的临床候选药物、针对目标适应症的正确剂量和方案至关重要。
本文回顾了现有的单克隆抗体文献和知识。具体来说,作者讨论了单克隆抗体的药代动力学(包括吸收、分布和消除)及其药效学。作者还研究了药代动力学/药效学关系,从临床前研究到临床研究的扩展以及首次人体剂量的选择。
单克隆抗体具有复杂的药代动力学和药效学特征,这些特征取决于多种因素。因此,从基础研究的角度提高我们对单克隆抗体药代动力学和药效学的理解非常重要。同样重要的是,应用机制药代动力学/药效学模型来解释实验结果,并有助于努力预测单克隆抗体的安全性和疗效。