群体药代动力学和药代动力学/药效学模型在药物开发和临床实践中的概念和应用

Q4 Pharmacology, Toxicology and Pharmaceutics
M. Roganović, A. Homšek, Marija Jovanović, Valentina Topić-Vučenović, M. Ćulafić, B. Miljković, K. Vučićević
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引用次数: 1

摘要

由于临床试验失败频繁,新药获批较少,基于模型的药物开发在一定程度上满足了改进药物开发的需要。药物计量学是药理学的一部分,它基于不同的模型(药代动力学- PK、药效学- PD、PK/PD模型等)和模拟来量化药物行为、治疗反应和疾病进展。监管机构(欧洲药品管理局,食品和药物管理局)鼓励使用建模和模拟,以促进整个药物开发阶段的决策。此外,确定导致变异的因素为常规临床实践中的剂量个体化提供了基础。这篇综述总结了目前关于药物计量学在药物开发和临床实践中的应用的知识,重点是人口建模方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Concept and utility of population pharmacokinetic and pharmacokinetic/pharmacodynamic models in drug development and clinical practice
Due to frequent clinical trial failures and consequently fewer new drug approvals, the need for improvement in drug development has, to a certain extent, been met using model-based drug development. Pharmacometrics is a part of pharmacology that quantifies drug behaviour, treatment response and disease progression based on different models (pharmacokinetic - PK, pharmacodynamic - PD, PK/PD models, etc.) and simulations. Regulatory bodies (European Medicines Agency, Food and Drug Administration) encourage the use of modelling and simulations to facilitate decision-making throughout all drug development phases. Moreover, the identification of factors that contribute to variability provides a basis for dose individualisation in routine clinical practice. This review summarises current knowledge regarding the application of pharmacometrics in drug development and clinical practice with emphasis on the population modelling approach.
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来源期刊
Arhiv za Farmaciju
Arhiv za Farmaciju Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
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发文量
19
审稿时长
12 weeks
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