Insights into Drug Development with Quantitative Systems Pharmacology: A Prospective Case Study of Uncovering Hyperkalemia Risk in Diabetic Nephropathy with Virtual Clinical Trials

医学 高钾血症 系统药理学 临床试验 药理学 疾病 依普利酮 重症监护医学 醛固酮 药品 内科学 螺内酯
作者
Véronique Baudrie,Tomohisa Nakada
出处
期刊:Drug Metabolism and Pharmacokinetics [Elsevier BV]
卷期号:56: 101019-101019
标识
DOI:10.1016/j.dmpk.2024.101019
摘要

The quantitative systems pharmacology (QSP) approach is widely applied to address various essential questions in drug discovery and development, such as identification of the mechanism of action of a therapeutic agent, patient stratification, and the mechanistic understanding of the progression of disease. In this review article, we show the current landscape of the application of QSP modeling using a survey of QSP publications over 10 years from 2013 to 2022. We also present a use case for the risk assessment of hyperkalemia in patients with diabetic nephropathy treated with mineralocorticoid receptor antagonists (MRAs, renin-angiotensin-aldosterone system inhibitors), as a prospective simulation of late clinical development. A QSP model for generating virtual patients with diabetic nephropathy was used to quantitatively assess that the nonsteroidal MRAs, finerenone and apararenone, have a lower risk of hyperkalemia than the steroidal MRA, eplerenone. Prospective simulation studies using a QSP model are useful to prioritize pharmaceutical candidates in clinical development and validate mechanism-based pharmacological concepts related to the risk-benefit, before conducting large-scale clinical trials.
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