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Modeling and simulation at the interface of nonclinical and early clinical drug development.

作者信息

Visser S A G, Manolis E, Danhof M, Kerbusch T

机构信息

1] Global DMPK, Innovative Medicines, AstraZeneca R&D, Södertälje, Sweden [2] Current affiliation: Merck Research Laboratories, Merck & Co., Inc., Upper Gwynedd, PA, USA.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2013 Feb 27;2(2):e30. doi: 10.1038/psp.2013.3.

DOI:10.1038/psp.2013.3
PMID:23835941
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3600756/
Abstract
摘要

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本文引用的文献

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The Role of Modeling and Simulation in Development and Registration of Medicinal Products: Output From the EFPIA/EMA Modeling and Simulation Workshop.模型和模拟在药品开发和注册中的作用:来自 EFPIA/EMA 模型和模拟研讨会的结果。
CPT Pharmacometrics Syst Pharmacol. 2013 Feb 27;2(2):e31. doi: 10.1038/psp.2013.7.
2
CPT: Pharmacometrics and Systems Pharmacology.CPT:药物代谢动力学与系统药理学。
CPT Pharmacometrics Syst Pharmacol. 2012 Sep 26;1(9):e8. doi: 10.1038/psp.2012.8.
3
Can the flow of medicines be improved? Fundamental pharmacokinetic and pharmacological principles toward improving Phase II survival.药物的传递能否得到改善?提高 II 期生存率的基础药代动力学和药理学原则。
Drug Discov Today. 2012 May;17(9-10):419-24. doi: 10.1016/j.drudis.2011.12.020. Epub 2011 Dec 29.
4
New pathway for qualification of novel methodologies in the European Medicines Agency.新的途径来确定欧洲药品管理局的新方法的资格。
Proteomics Clin Appl. 2011 Jun;5(5-6):248-55. doi: 10.1002/prca.201000130. Epub 2011 Apr 28.
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Systems biology and pharmacology.系统生物学与药理学。
Clin Pharmacol Ther. 2010 Jul;88(1):17-9. doi: 10.1038/clpt.2010.69.
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Annu Rev Pharmacol Toxicol. 2007;47:357-400. doi: 10.1146/annurev.pharmtox.47.120505.105154.