Pharmacokinetics of Enarodustat in Non-Japanese and Japanese Healthy Subjects and in Patients With End-Stage Renal Disease on Hemodialysis

被引:4
作者
Pai, Sudhakar M. [1 ,3 ]
Kambhampati, Siva Rama Prasad [1 ]
Naruhashi, Shinya [2 ]
Yamada, Hiroyuki [2 ]
机构
[1] Akros Pharm Inc, Clin Pharmacol, Princeton, NJ USA
[2] Japan Tobacco Inc, Pharmaceut Div, Clin Pharmacol, Tokyo, Japan
[3] Akros Pharm Inc, 302 Carnegie Ctr, Princeton, NJ 08540 USA
关键词
clinical pharmacology; enarodustat; ESRD; hemodialysis; HIF-PH; JTZ-951; pharmacokinetics;
D O I
10.1002/cpdd.1252
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The pharmacokinetics of enarodustat were elucidated in healthy subjects and in patients with end-stage renal disease (ESRD) on hemodialysis in phase 1 studies conducted in the United States and Japan. In healthy non-Japanese and Japanese subjects, following single oral administration up to 400 mg, enarodustat was rapidly absorbed. Maximum plasma concentration and area under the plasma concentration-time curve from the time of dosing to infinity were dose-dependent, renal excretion of unchanged enarodustat was substantial (on average approximate to 45% of dose), and mean t(1/2) of <10 hours indicated negligible accumulation with once-daily dosing. In general, with daily dosing (25, 50 mg), accumulation at steady-state was approximate to 1.5-fold (t(1/2(eff)) approximate to 15 hours), presumably due to a decrease in renal drug excretion which is not clinically relevant in patients with ESRD. In the single- and multiple-dose studies, plasma clearance (CL/F) was lower in healthy Japanese subjects. In non-Japanese patients with ESRD on hemodialysis, following once-daily dosing (2-15 mg), enarodustat was rapidly absorbed, steady-state maximum plasma concentration and area under the plasma concentration-time curve during the dosing interval were dose-dependent, and interindividual variability in the exposure parameters was low-to-moderate (coefficient of variation, 27%-39%). Steady-state CL/F was similar across doses, renal drug excretion was not significant (<10% of dose), mean t(1/2) and t(1/2(eff)) were similar (overall, 8.97-11.6 hours), and accumulation was minimal (approximate to 20%), demonstrating predictable pharmacokinetics. Japanese patients with ESRD on hemodialysis (15 mg, single dose) exhibited similar pharmacokinetics with mean t(1/2) of 11.3 hours and low interindividual variability in the exposure parameters, albeit with lower CL/F versus non-Japanese patients. Body weight-adjusted clearance values were generally similar in non-Japanese and Japanese healthy subjects and also in patients with ESRD on hemodialysis.
引用
收藏
页码:683 / 690
页数:8
相关论文
共 10 条
[1]   Serum erythropoietin concentrations and responses to anaemia in patients with or without chronic kidney disease [J].
Artunc, Ferruh ;
Risler, Teut .
NEPHROLOGY DIALYSIS TRANSPLANTATION, 2007, 22 (10) :2900-2908
[2]   EFFECTIVE HALF-LIFE IN CLINICAL-PHARMACOLOGY [J].
BOXENBAUM, H ;
BATTLE, M .
JOURNAL OF CLINICAL PHARMACOLOGY, 1995, 35 (08) :763-766
[3]   Hypoxia and the HIF system in kidney disease [J].
Nangaku, Masaomi ;
Eckardt, Kai-Uwe .
JOURNAL OF MOLECULAR MEDICINE-JMM, 2007, 85 (12) :1325-1330
[4]   Pathogenesis of renal anemia [J].
Nangaku, Masaomi ;
Eckardt, Kai-Uwe .
SEMINARS IN NEPHROLOGY, 2006, 26 (04) :261-268
[5]   Discovery of JTZ-951: A HIF Prolyl Hydroxylase Inhibitor for the Treatment of Renal Anemia [J].
Ogoshi, Yosuke ;
Matsui, Takuya ;
Mitani, Ikuo ;
Yokota, Masahiro ;
Terashita, Masakazu ;
Motoda, Dai ;
Ueyama, Kazuhito ;
Hotta, Takahiro ;
Ito, Takashi ;
Hase, Yasunori ;
Fukui, Kenji ;
Deai, Katsuya ;
Yoshiuchi, Hiromi ;
Ito, Soichiro ;
Abe, Hiroyuki .
ACS MEDICINAL CHEMISTRY LETTERS, 2017, 8 (12) :1320-1325
[6]   A highly sensitive and selective UPLC-MS/MS assay for the determination of enarodustat (JTZ-951) in human plasma [J].
Pai, Sudhakar ;
Huang, Mike Qingtao ;
Maki, Koichi ;
Waldron, Michael ;
Yoshikawa, Tomonori ;
Keller, Tara ;
Burnett, James .
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES, 2021, 1176
[7]   Hemodialysis Clearance of Enarodustat (JTZ-951), an Oral Erythropoiesis Stimulating Agent, in Patients with End-Stage Renal Disease [J].
Pai, Sudhakar M. ;
Yamada, Hiroyuki .
CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2021, 10 (05) :463-470
[8]   A Mass Balance Study of 14C-Labeled JTZ-951 (Enarodustat), a Novel Orally Available Erythropoiesis-Stimulating Agent, in Patients With End-Stage Renal Disease on Hemodialysis [J].
Pai, Sudhakar M. ;
Connaire, Jeffrey ;
Yamada, Hiroyuki ;
Enya, Seiji ;
Gerhardt, Barbara ;
Maekawa, Michihide ;
Tanaka, Hiromasa ;
Koretomo, Ryosuke ;
Ishikawa, Tomohiro .
CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT, 2020, 9 (06) :728-741
[9]   A gain-of-function mutation in the HIF2A gene in familial erythrocytosis [J].
Percy, Melanie J. ;
Furlow, Paul W. ;
Lucas, Guy S. ;
Li, Xiping ;
Lappin, Terence R. J. ;
McMullin, Mary Frances ;
Lee, Frank S. .
NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (02) :162-168
[10]  
Suzuki S., 2009, KIDNEY DIALYSIS, V67, P531