Pharmacokinetic and Pharmacodynamic Modeling of MOD-4023, a Long-Acting Human Growth Hormone, in Growth Hormone Deficiency Children

被引:31
|
作者
Fisher, Dennis M. [1 ]
Rosenfeld, Ron G. [2 ]
Jaron-Mendelson, Michal [3 ]
Amitzi, Leanne [3 ]
Koren, Ronit [3 ]
Hart, Gili [3 ]
机构
[1] P Less Than, 218 Castenada Ave, San Francisco, CA 94116 USA
[2] Stat5 Consulting LLC, Los Altos, CA USA
[3] OPKO Biol, Kiryat Gat, Israel
来源
HORMONE RESEARCH IN PAEDIATRICS | 2017年 / 87卷 / 05期
关键词
Growth hormone; Growth hormone deficiency; Growth hormone replacement; Growth in children; Insulin growth factor 1; Long-acting growth hormone; Weekly growth hormone; Pharmacokinetic/pharmacodynamic modeling; I IGF-I;
D O I
10.1159/000470842
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background/Aims: MOD-4023 is a long-acting human growth hormone (hGH) in clinical trials for the treatment of growth hormone deficiency (GHD). A key goal is maintenance of serum concentrations of insulin-like growth factor (IGF) 1 within normal range throughout GH dosing. The study aimed to develop a pharmacokinetic model for MOD-4023 and a pharmacodynamic model for the effect of MOD-4023 on IGF-1 to allow estimation of peak and mean IGF-1 and to identify the optimal IGF-1 sampling day. Methods: MOD-4023 (0.25, 0.48, or 0.66 mg/kg) was administered weekly for 12 months to 41 GH-naive GHD children (age 3-11 years). The control group (n = 11, age 4-9 years) received daily recombinant human growth hormone (r-hGH; 34 mu g/kg). Sparse samples (4/subject) were obtained to determine serum concentrations of MOD-4023 or r-hGH and IGF-1. Results: A 2-compartment pharmacokinetic model with first-order absorption fit MOD-4023 data well; a 1-compartment model was appropriate for r-hGH. For both, weight-normalized systemic parameters were preferred over allometric scaling. For MOD-4023, an indirect model fit IGF-1 SDS data well; baseline IGF-1 increased over time. At steady state, samples obtained 4 days following dose administration predicted mean IGF-1 SDS during the dosing interval well. Conclusion: The IGF-1 profile is consistent with the weekly dosing interval. Sampling 4 days following dose administration allows estimation of mean IGF-1 SDS during the dosing interval in GHD patients. (C) 2017 The Author(s) Published by S. Karger AG, Basel
引用
收藏
页码:324 / 332
页数:9
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