共 5 条
Insights into drug development with quantitative systems pharmacology: A prospective case study of uncovering hyperkalemia risk in diabetic nephropathy with virtual clinical trials
被引:1
|作者:
Saito, Ryuta
[1
,2
]
Nakada, Tomohisa
[1
]
机构:
[1] Mitsubishi Tanabe Pharm Corp, Discovery Technol Labs, Sohyaku Innovat Res Div, Yokohama 2270033, Japan
[2] Mitsubishi Tanabe Pharm Corp, 1000, Kamoshida-cho, Aoba-ku, Yokohama 2270033, Japan
关键词:
Quantitative systems pharmacology;
Model-informed drug discovery and;
development;
Clinical trial simulation;
Diabetic nephropathy;
Hyperkalemia;
Renin-angiotensin-aldosterone system;
inhibitor;
Mineralocorticoid receptor antagonist;
MINERALOCORTICOID RECEPTOR ACTIVATION;
ARTERIAL-PRESSURE;
ALDOSTERONE;
HYPERTENSION;
ALBUMINURIA;
MECHANISMS;
BLOCKADE;
D O I:
10.1016/j.dmpk.2024.101019
中图分类号:
R9 [药学];
学科分类号:
1007 ;
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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页数:8
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