MedImmune, Mountain View, California, USA.
MedImmune, Cambridge, UK.
CPT Pharmacometrics Syst Pharmacol. 2018 Jan;7(1):5-15. doi: 10.1002/psp4.12245. Epub 2017 Nov 23.
Drug development is a lengthy, costly process with low probability of success. Biopharmaceuticals are highly specific molecules, with efficacy and safety closely tied to target biology and pharmacology. The "learning-predicting-confirming" continuum by translational and clinical modeling and simulation (M&S) was implemented at every decision point for mavrilimumab, a human monoclonal antibody in development for rheumatoid arthritis (RA). This tutorial uses mavrilimumab as an example to demonstrate rational discovery, preclinical development, clinical study design, and dose selection of biotherapeutics by M&S.
药物研发是一个漫长且昂贵的过程,成功率较低。生物制药是高度特异的分子,其疗效和安全性与靶标生物学和药理学密切相关。在类风湿关节炎(RA)治疗药物 mavrilimumab 的开发过程中,通过转化和临床建模与仿真(M&S)的“学习-预测-确认”连续体,在每个决策点都进行了实施。本教程以 mavrilimumab 为例,演示了通过 M&S 进行生物治疗药物的合理发现、临床前开发、临床研究设计和剂量选择。