A Single-Dose, Open-Label, Randomized, Two-Way Crossover Study in Healthy Japanese Participants to Evaluate the Bioequivalence and the Food Effect on the Pharmacokinetics of Daprodustat

被引:7
|
作者
Yamada, Masanori [1 ]
Osamura, Minori [1 ]
Ogura, Hirofumi [1 ]
Onoue, Tomohiro [2 ]
Wakamatsu, Akira [3 ]
Numachi, Yotaro [4 ]
Caltabiano, Stephen [5 ]
Mahar, Kelly M. [6 ]
机构
[1] GlaxoSmithKline KK, Japan Dev Div, Clin Pharmacol Off, Tokyo, Japan
[2] GlaxoSmithKline KK, Japan Dev Div, Biomed Data Sci Dept, Tokyo, Japan
[3] GlaxoSmithKline KK, Japan Dev Div, Preclin Dev Dept, Tokyo, Japan
[4] GlaxoSmithKline KK, Japan Dev Div, Med Dev, Tokyo, Japan
[5] GlaxoSmithKline, Clin Dev, Collegeville, PA USA
[6] GlaxoSmithKline, Clin Pharmacol Modeling & Simulat, Collegeville, PA USA
来源
CLINICAL PHARMACOLOGY IN DRUG DEVELOPMENT | 2020年 / 9卷 / 08期
关键词
bioequivalence; daprodustat; food effect; healthy subject; Japanese; pharmacokinetics; safety; single dose; PROLYL HYDROXYLASE INHIBITOR; GSK1278863; HYPOXIA;
D O I
10.1002/cpdd.793
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Daprodustat is a prolyl hydroxylase inhibitor that stimulates erythropoiesis in a manner similar to the natural response to hypoxia, whereby inhibition of hypoxia inducible factor (HIF) prolyl-4-hydroxylases by daprodustat ultimately results in increased levels of HIF-responsive genes. Daprodustat is under development as an emerging new class of agents for the treatment of anemia associated with chronic kidney disease (CKD). This was a single-center, single-dose, open-label, randomized, 2-way crossover study in healthy Japanese male participants consisting of 2 parts. The primary objective was to evaluate the bioequivalence (BE) between daprodustat tablet strengths (part 1) and to evaluate the food effect on the pharmacokinetics (PK) of daprodustat (part 2). A total of 64 healthy Japanese male participants were enrolled; 52 participants were included in part 1 and 12 in part 2. BE was demonstrated between the daprodustat 2-mg tablet and the daprodustat 4-mg tablet. A standard CKD meal did not have a large effect on the PK parameters of daprodustat after a single oral dose of daprodustat 4 mg. Administration of single oral doses of daprodustat 4 mg was generally well tolerated in the healthy Japanese participants, and no new safety signals were identified without regard to food.
引用
收藏
页码:978 / 984
页数:7
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