Pharmacokinetics of Macitentan in Caucasian and Japanese Subjects: The Influence of Ethnicity and Sex

被引:34
作者
Bruderer, Shirin [1 ]
Marjason, Joanne [2 ]
Sidharta, Patricia N. [1 ]
Dingemanse, Jasper [1 ]
机构
[1] Actel Pharmaceut Ltd, Dept Clin Pharmacol, CH-4123 Allschwil, Switzerland
[2] Q Pharm Pty Ltd, Herston, Qld, Australia
关键词
Macitentan; Caucasian and Japanese subjects; Pharmacokinetics; Sex; ENDOTHELIN RECEPTOR ANTAGONIST; GENETIC POLYMORPHISMS; DRUG-METABOLISM; PHARMACODYNAMICS; TOLERABILITY; WARFARIN; HUMANS; RACE;
D O I
10.1159/000351704
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Background/Aims: Macitentan is a novel dual endothelin receptor antagonist with sustained receptor binding in clinical development for pulmonary arterial hypertension. The present study compared the pharmacokinetics and safety of macitentan in healthy Caucasian and Japanese subjects and explored the potential sex differences. Methods: In this single-center, open-label, phase I study 10 healthy subjects of each ethnic origin with a male/female ratio of 1:1 in each group were administered a single oral 10-mg dose of macitentan. Blood samples were taken to determine plasma levels of macitentan and its pharmacologically active metabolite, ACT-132577, and safety and tolerability were monitored using standard assessments. Results: For both macitentan and its metabolite, values for C-max were similar but a shorter half-life was determined in Japanese subjects resulting in an exposure to both compounds being approximately 15% lower in Japanese when compared to Caucasian subjects. The exposure to macitentan was similar in Japanese males and females whereas Caucasian females had an approximately 25% higher exposure than Caucasian males. In both ethnic groups, females had an approximately 15% higher exposure to ACT-132577 than male subjects. Macitentan was well tolerated in both ethnic groups. There were no clinically significant differences in adverse event profile, clinical laboratory, electrocardiographic parameters, and vital signs between both groups. Conclusion: The data suggest that the minor differences in pharmacokinetics between the two groups are not clinically relevant and no dose adjustment of macitentan based on Japanese ethnic origin or sex is necessary. Copyright (C) 2013 S. Karger AG, Basel
引用
收藏
页码:331 / 338
页数:8
相关论文
共 30 条
[1]   Gender differences in pharmacological response [J].
Anderson, Gail D. .
EPILEPSY IN WOMEN: THE SCIENTIFIC BASIS FOR CLINICAL MANAGEMENT, 2008, 83 :1-10
[2]   A review and assessment of potential sources of ethnic differences in drug responsiveness [J].
Bjornsson, TD ;
Wagner, JA ;
Donahue, SR ;
Harper, D ;
Karim, A ;
Khouri, MS ;
Murphy, WR ;
Roman, K ;
Schneck, D ;
Sonnichsen, DS ;
Stalker, DJ ;
Wise, SD ;
Dombey, S ;
Loew, C .
JOURNAL OF CLINICAL PHARMACOLOGY, 2003, 43 (09) :943-967
[3]   The Discovery of N-[5-(4-Bromophenyl)-6-[2-[(5-bromo-2-pyrimidinyl)oxy]ethoxy]-4-pyrimidinyl]-N′-propylsulfamide (Macitentan), an Orally Active, Potent Dual Endothelin Receptor Antagonist [J].
Bolli, Martin H. ;
Boss, Christoph ;
Binkert, Christoph ;
Buchmann, Stephan ;
Bur, Daniel ;
Hess, Patrick ;
Iglarz, Marc ;
Meyer, Solange ;
Rein, Josiane ;
Rey, Markus ;
Treiber, Alexander ;
Clozel, Martine ;
Fischli, Walter ;
Weller, Thomas .
JOURNAL OF MEDICINAL CHEMISTRY, 2012, 55 (17) :7849-7861
[4]   Absorption, distribution, metabolism, and excretion of macitentan, a dual endothelin receptor antagonist, in humans [J].
Bruderer, Shirin ;
Hopfgartner, Gerard ;
Seiberling, Michael ;
Wank, Janine ;
Sidharta, Patricia N. ;
Treiber, Alexander ;
Dingemanse, Jasper .
XENOBIOTICA, 2012, 42 (09) :901-910
[5]   Effect of Cyclosporine and Rifampin on the Pharmacokinetics of Macitentan, a Tissue-Targeting Dual Endothelin Receptor Antagonist [J].
Bruderer, Shirin ;
Aeaenismaa, Paeivi ;
Homery, Marie-Claude ;
Haeusler, Stephanie ;
Landskroner, Kyle ;
Sidharta, Patricia N. ;
Treiber, Alexander ;
Dingemanse, Jasper .
AAPS JOURNAL, 2012, 14 (01) :68-78
[6]  
Daly AK, 2012, ADV PHARMACOL, V63, P137, DOI 10.1016/B978-0-12-398339-8.00004-5
[7]   Part 2: Pharmacogenetic Variability in Drug Transport and Phase I Anticancer Drug Metabolism [J].
Deenen, Maarten J. ;
Cats, Annemieke ;
Beijnen, Jos H. ;
Schellens, Jan H. M. .
ONCOLOGIST, 2011, 16 (06) :820-834
[8]   Comparison of the pharmacokinetics, pharmacodynamics and tolerability of tezosentan between caucasian and Japanese subjects [J].
Dingemanse, J ;
Gunawardena, KA ;
van Giersbergen, PLM .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2006, 61 (04) :405-413
[9]  
European Medicines Agency, 2010, CPMPQWPEWP140198
[10]  
Evelyn B, 2001, J NATL MED ASSOC, V93, p18S