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
相关论文
共 10 条
[1]   Reference Intervals for Insulin-like Growth Factor-1 (IGF-I) From Birth to Senescence: Results From a Multicenter Study Using a New Automated Chemiluminescence IGF-I Immunoassay Conforming to Recent International Recommendations [J].
Bidlingmaier, Martin ;
Friedrich, Nele ;
Emeny, Rebecca T. ;
Spranger, Joachim ;
Wolthers, Ole D. ;
Roswall, Josefine ;
Koerner, Antje ;
Obermayer-Pietsch, Barbara ;
Huebener, Christoph ;
Dahlgren, Jovanna ;
Frystyk, Jan ;
Pfeiffer, Andreas F. H. ;
Doering, Angela ;
Bielohuby, Maximilian ;
Wallaschofski, Henri ;
Arafat, Ayman M. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2014, 99 (05) :1712-1721
[2]   Growth Hormone Research Society perspective on the development of long-acting growth hormone preparations [J].
Christiansen, Jens Sandahl ;
Backeljauw, Philippe F. ;
Bidlingmaier, Martin ;
Biller, Beverly M. K. ;
Boguszewski, Margaret C. S. ;
Casanueva, Felipe F. ;
Chanson, Philippe ;
Chatelain, Pierre ;
Choong, Catherine S. ;
Clemmons, David R. ;
Cohen, Laurie E. ;
Cohen, Pinchas ;
Frystyk, Jan ;
Grimberg, Adda ;
Hasegawa, Yukihiro ;
Haymond, Morey W. ;
Ho, Ken ;
Hoffman, Andrew R. ;
Holly, Jeff M. P. ;
Horikawa, Reiko ;
Hoeybye, Charlotte ;
Jorgensen, Jens Otto L. ;
Johannsson, Gudmundur ;
Juul, Anders ;
Katznelson, Laurence ;
Kopchick, John J. ;
Lee, K. O. ;
Lee, Kuk-Wha ;
Luo, Xiaoping ;
Melmed, Shlomo ;
Miller, Bradley S. ;
Misra, Madhusmita ;
Popovic, Vera ;
Rosenfeld, Ron G. ;
Ross, Judith ;
Ross, Richard J. ;
Saenger, Paul ;
Strasburger, Christian J. ;
Thorner, Michael O. ;
Werner, Haim ;
Yuen, Kevin .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2016, 174 (06) :C1-C8
[3]   Reference ranges for two automated chemiluminescent assays for serum insulin-like growth factor I (IGF-I) and IGF-binding protein 3 (IGFBP-3) [J].
Elmlinger, MW ;
Kühnel, W ;
Weber, MM ;
Ranke, MB .
CLINICAL CHEMISTRY AND LABORATORY MEDICINE, 2004, 42 (06) :654-664
[4]   Observations of nonadherence to recombinant human growth hormone therapy in clinical practice [J].
Haverkamp, Fritz ;
Johansson, Lotta ;
Dumas, Herve ;
Langham, Shirley ;
Tauber, Maithe ;
Veimo, Dag ;
Chiarelli, Francesco .
CLINICAL THERAPEUTICS, 2008, 30 (02) :307-316
[5]   In Vitro and in Vivo Characterization of MOD-4023, a Long-Acting Carboxy-Terminal Peptide (CTP)-Modified Human Growth Hormone [J].
Hershkovitz, Oren ;
Bar-Ilan, Ahuva ;
Guy, Rachel ;
Felikman, Yana ;
Moschcovich, Laura ;
Hwa, Vivian ;
Rosenfeld, Ron G. ;
Fima, Eyal ;
Hart, Gili .
MOLECULAR PHARMACEUTICS, 2016, 13 (02) :631-639
[6]  
Israel E, 2000, J CLIN ENDOCR METAB, V85, P3990
[7]  
SCHWARTZ GJ, 1976, PEDIATRICS, V58, P259
[8]   MOD-4023, a long-acting carboxy-terminal peptide-modified human growth hormone: results of a Phase 2 study in growth hormone-deficient adults [J].
Strasburger, Christian J. ;
Vanuga, Peter ;
Payer, Juraj ;
Pfeifer, Marija ;
Popovic, Vera ;
Bajnok, Laszlo ;
Goth, Miklos ;
Olsovska, Vera ;
Trejbalova, Ludmila ;
Vadasz, Janos ;
Fima, Eyal ;
Koren, Ronit ;
Amitzi, Leanne ;
Bidlingmaier, Martin ;
Hershkovitz, Oren ;
Hart, Gili ;
Biller, Beverly M. K. .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2017, 176 (03) :283-294
[9]  
Sun YN, 1999, J PHARMACOL EXP THER, V289, P1523
[10]  
Zelinska N, 2017, J CLIN ENDOCR METAB, V102, P1