A Bayesian K-PD model for synergy: A case study

被引:4
作者
La Gamba, Fabiola [1 ,2 ]
Jacobs, Tom [1 ]
Geys, Helena [1 ,2 ]
Ver Donck, Luc [1 ]
Faes, Christel [2 ]
机构
[1] Janssen Res & Dev, Turnhoutseweg 30, B-2340 Beerse, Belgium
[2] Hasselt Univ, I BioStat, Agoralaan Bldg D, B-3590 Diepenbeek, Belgium
基金
欧盟地平线“2020”;
关键词
Bayesian inference; coadministration; indirect response model; pharmacodynamics; pharmacokinetics; INDIRECT PHARMACODYNAMIC RESPONSES; 4 BASIC MODELS; DRUG; KINETICS;
D O I
10.1002/pst.1887
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Coadministration of 2 or more compounds can alter both the pharmacokinetics and pharmacodynamics of individual compounds. While experiments on pharmacodynamic drug-drug interactions are usually performed in an in vitro setting, this experiment focuses on an in vivo setting. The change over time of a safety biomarker is modeled using an indirect response model, in which the virtual pharmacokinetic profile of one compound drives the effect of the other. Several experiments at different dose level combinations were performed sequentially. While a traditional frequentist analysis consists of estimating the model parameters based on all the data simultaneously, in this work, we consider a Bayesian inference framework allowing to incorporate the results from a historical dose-response experiment.
引用
收藏
页码:674 / 684
页数:11
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