Novadiscovery SA, Lyon, France.
Methods Mol Biol. 2024;2716:51-99. doi: 10.1007/978-1-0716-3449-3_4.
Modeling and simulation (M&S), including in silico (clinical) trials, helps accelerate drug research and development and reduce costs and have coined the term "model-informed drug development (MIDD)." Data-driven, inferential approaches are now becoming increasingly complemented by emerging complex physiologically and knowledge-based disease (and drug) models, but differ in setup, bottlenecks, data requirements, and applications (also reminiscent of the different scientific communities they arose from). At the same time, and within the MIDD landscape, regulators and drug developers start to embrace in silico trials as a potential tool to refine, reduce, and ultimately replace clinical trials. Effectively, silos between the historically distinct modeling approaches start to break down. Widespread adoption of in silico trials still needs more collaboration between different stakeholders and established precedence use cases in key applications, which is currently impeded by a shattered collection of tools and practices. In order to address these key challenges, efforts to establish best practice workflows need to be undertaken and new collaborative M&S tools devised, and an attempt to provide a coherent set of solutions is provided in this chapter. First, a dedicated workflow for in silico clinical trial (development) life cycle is provided, which takes up general ideas from the systems biology and quantitative systems pharmacology space and which implements specific steps toward regulatory qualification. Then, key characteristics of an in silico trial software platform implementation are given on the example of jinkō.ai (nova's end-to-end in silico clinical trial platform). Considering these enabling scientific and technological advances, future applications of in silico trials to refine, reduce, and replace clinical research are indicated, ranging from synthetic control strategies and digital twins, which overall shows promise to begin a new era of more efficient drug development.
建模与仿真(M&S),包括计算机临床试验,有助于加速药物研发并降低成本,因此创造了“模型引导的药物研发(MIDD)”一词。基于数据的推理方法现在越来越多地与新兴的复杂生理和基于知识的疾病(和药物)模型相辅相成,但在设置、瓶颈、数据要求和应用方面存在差异(这也让人联想到它们所源自的不同科学领域)。与此同时,在 MIDD 领域,监管机构和药物开发商开始将计算机临床试验作为一种潜在的工具来改进、减少,最终取代临床试验。实际上,历史上不同建模方法之间的隔阂开始打破。要广泛采用计算机临床试验,还需要不同利益相关者之间进行更多的合作,并在关键应用中建立既定的先例用例,而这目前受到破碎的工具和实践集合的阻碍。为了解决这些关键挑战,需要努力建立最佳实践工作流程,并设计新的协作 M&S 工具,并在本章中尝试提供一套连贯的解决方案。首先,提供了专门用于计算机临床试验(开发)生命周期的工作流程,该流程借鉴了系统生物学和定量系统药理学领域的一般思想,并朝着监管资格的特定步骤实施。然后,以 jinkō.ai(nova 的端到端计算机临床试验平台)为例,介绍了计算机试验软件平台实现的关键特征。考虑到这些使能的科学和技术进步,未来将计算机临床试验应用于改进、减少和替代临床研究的应用范围很广,从合成控制策略和数字孪生,这总体上有望开启一个更高效药物研发的新时代。