Translational Disease Modeling, Translational Medicine and Early Development, Sanofi US, Bridgewater, New Jersey, USA.
Clin Pharmacol Ther. 2024 Dec;116(6):1442-1451. doi: 10.1002/cpt.3451. Epub 2024 Sep 28.
Rare diseases, affecting millions globally, present significant drug development challenges. This is due to the limited patient populations and the unique pathophysiology of these diseases, which can make traditional clinical trial designs unfeasible. Quantitative Systems Pharmacology (QSP) models offer a promising approach to expedite drug development, particularly in rare diseases. QSP models provide a mechanistic representation of the disease and drug response in virtual patients that can complement routinely applied empirical modeling and simulation approaches. QSP models can generate digital twins of actual patients and mechanistically simulate the disease progression of rare diseases, accounting for phenotypic heterogeneity. QSP models can also support drug development in various drug modalities, such as gene therapy. Impactful QSP models case studies are presented here to illustrate their value in supporting various aspects of drug development in rare indications. As these QSP model applications continue to mature, there is a growing possibility that they could be more widely integrated into routine drug development steps. This integration could provide a robust framework for addressing some of the inherent challenges in rare disease drug development.
罕见病影响着全球数百万人,给药物研发带来了巨大挑战。这是因为这些疾病的患者群体有限,病理生理学独特,使得传统的临床试验设计变得不可行。定量系统药理学 (QSP) 模型为加速药物研发提供了一种很有前途的方法,尤其是在罕见病领域。QSP 模型为虚拟患者的疾病和药物反应提供了一种机制化的描述,可以补充常规应用的经验模型和模拟方法。QSP 模型可以生成实际患者的数字双胞胎,并对罕见疾病的疾病进展进行机制模拟,同时考虑表型异质性。QSP 模型还可以支持各种药物模式(如基因治疗)的药物研发。本文介绍了一些有影响力的 QSP 模型案例研究,以说明它们在支持罕见适应症药物研发各个方面的价值。随着这些 QSP 模型应用的不断成熟,它们越来越有可能被更广泛地整合到常规药物研发步骤中。这种整合为解决罕见病药物研发中的一些固有挑战提供了一个强大的框架。