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.
引用
收藏
页数:8
相关论文
共 5 条
  • [1] Algorithms and methodological challenges in the development and application of quantitative systems pharmacology models: a case study in type 2 diabetes
    Sokolov, Victor
    RUSSIAN JOURNAL OF NUMERICAL ANALYSIS AND MATHEMATICAL MODELLING, 2022, 37 (05) : 293 - 309
  • [2] Assessing Bladder Cancer Risk in Type 2 Diabetes Clinical Trials: the Dapagliflozin Drug Development Program as a 'Case Study'
    Ptaszynska, Agata
    Cohen, Samuel M.
    Messing, Edward M.
    Reilly, Timothy P.
    Johnsson, Eva
    Johnsson, Kristina
    DIABETES THERAPY, 2015, 6 (03) : 357 - 375
  • [3] FDA-Industry Scientific Exchange on assessing quantitative systems pharmacology models in clinical drug development: a meeting report, summary of challenges/gaps, and future perspective
    Bai, Jane P. F.
    Schmidt, Brian J.
    Gadkar, Kapil G.
    Damian, Valeriu
    Earp, Justin C.
    Friedrich, Christina
    van der Graaf, Piet H.
    Madabushi, Rajanikanth
    Musante, Cynthia J.
    Naik, Kunal
    Rogge, Mark
    Zhu, Hao
    AAPS JOURNAL, 2021, 23 (03):
  • [4] FDA-Industry Scientific Exchange on assessing quantitative systems pharmacology models in clinical drug development: a meeting report, summary of challenges/gaps, and future perspective
    Jane P. F. Bai
    Brian J. Schmidt
    Kapil G. Gadkar
    Valeriu Damian
    Justin C. Earp
    Christina Friedrich
    Piet H. van der Graaf
    Rajanikanth Madabushi
    Cynthia J. Musante
    Kunal Naik
    Mark Rogge
    Hao Zhu
    The AAPS Journal, 23
  • [5] Is low birth weight a risk factor for the development of diabetic nephropathy in patients with type 1 diabetes? A population-based case-control study
    Eshoj, O
    Vaag, A
    Borch-Johnsen, K
    Feldt-Rasmussen, B
    Beck-Nielsen, H
    JOURNAL OF INTERNAL MEDICINE, 2002, 252 (06) : 524 - 528