Optimal Design for Multiresponse Pharmacokinetic–Pharmacodynamic Models – Dealing with Unbalanced Designs

被引:2
作者
Kayode Ogungbenro
Ivelina Gueorguieva
Oneeb Majid
Gordon Graham
Leon Aarons
机构
[1] The University of Manchester,Centre for Applied Pharmacokinetic Research
[2] Lilly Research Centre,School of Pharmacy and Pharmaceutical Sciences
[3] Global PK/PD,undefined
[4] Erl Wood Manor,undefined
[5] Pfizer Limited,undefined
[6] The University of Manchester,undefined
来源
Journal of Pharmacokinetics and Pharmacodynamics | 2007年 / 34卷
关键词
pharmacokinetics; pharmacodynamics; D-optimality; optimal design; multiresponse; nonlinear; fixed effects; mixed effects;
D O I
暂无
中图分类号
学科分类号
摘要
This paper addresses the problem of determining D-optimal designs for multiresponse pharmacokinetic–pharmacodynamic (PKPD) experiments where data on each response variable can be collected at different times. Most previous multiresponse model optimal design applications have considered the case where all response variables are measured at the same time points. However in practice it may not be possible to have all responses measured at the same sampling times. We propose an optimal design method to take into account the unbalanced nature of the problem. The method developed was applied to a PKPD problem that involved describing the time course of drug plasma concentrations, heart rate and mean arterial blood pressure for both a fixed effects and mixed effects regression model. Additionally a simulation study was carried out in NONMEM for one such population optimal design problem.
引用
收藏
页码:313 / 331
页数:18
相关论文
共 55 条
  • [1] Holford N.H.(1982)Kinetics of pharmacologic response Pharmacol. Ther. 16 143-166
  • [2] Sheiner L.B.(1991)Population pharmacokinetics: theory and practice Br. J. Clin. Pharmacol. 32 669-670
  • [3] Aarons L.(1992)Population pharmacokinetics Int. J. Clin. Pharmacol. Ther. Toxicol 30 520-522
  • [4] Aarons L.(1999)Software for population pharmacokinetics and pharmacodynamics Clin. Pharmacokinet. 36 255-264
  • [5] Aarons L.(1994)Population pharmacokinetic/pharmacodynamic methodology and applications: a bibliography Biometrics 50 566-575
  • [6] Yuh L.(1981)Optimal sampling times for pharmacokinetic experiments J. Pharmacokinet. Biopharm. 9 739-756
  • [7] Beal S.(2004)POPED, a software for optimal experiment design in population kinetics Comput. Methods Programs Biomed. 74 29-46
  • [8] Davidian M.(2002)The use of simulated annealing for finding optimal population designs Comput. Methods Programs Biomed. 69 25-35
  • [9] Harrison F.(2001)Development and implementation of the population Fisher information matrix for the evaluation of population pharmacokinetic designs Comput. Methods Programs Biomed. 65 141-151
  • [10] Hester A.(2002)Fisher information matrix for non-linear mixed-effects models: evaluation and application for optimal design of enoxaparin population pharmacokinetics Stat. Med. 21 2623-2639