Population Pharmacokinetics of the Novel Adenosine A2A Antagonist/Inverse Agonist KW-6356 and Its Active Metabolite Following Single and Multiple Oral Administration in Healthy Individuals and Patients with Parkinson's Disease

被引:1
|
作者
Tayama, Tomonori [1 ,2 ,4 ]
Okada, Hiroki [3 ]
Ogawa, Kotoko [1 ]
Marsteller, Douglas [3 ]
Maeda, Hiroshi [1 ]
Hruska, Matthew W. [3 ]
Kagawa, Yoshiyuki [2 ]
机构
[1] Kyowa Kirin Co Ltd, Clin Pharmacol, Tokyo, Japan
[2] Univ Shizuoka, Sch Pharmaceut Sci, Lab Clin Pharmaceut, Shizuoka, Japan
[3] Kyowa Kirin Inc, Clin Pharmacol, Princeton, NJ USA
[4] Kyowa Kirin Co Ltd, R&D Div, Clin Pharmacol, 1-9-2 Otemachi,Chiyoda Ku, Tokyo 1000004, Japan
来源
关键词
adenosine A(2A); adenosine antagonist; Parkinson's disease; KW-6356; population pharmacokinetics; metabolite; MODEL;
D O I
10.1002/cpdd.1359
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
KW-6356 is a selective antagonist and inverse agonist of the adenosine A(2A) receptor. The primary aim of the present analysis was to characterize the pharmacokinetics (PK) of KW-6356 and its active metabolite M6 in healthy subjects and patients with Parkinson's disease (PD). We pooled concentration-time data from healthy subjects and patients with PD who were administered KW-6356. Using these data, we developed a population PK model by sequentially fitting the KW-6356 parameters followed by the M6 parameters. A first-order absorption with a 1-compartment model for KW-6356 and a 1-compartment model for M6 best described the profiles. The covariates included in the final models were food status (fed/fasted/unknown) on first-order absorption rate constant, baseline serum albumin level on apparent clearance of KW-6356, and baseline body weight on apparent volume of distribution of KW-6356 and apparent clearance of M6. No covariate had a clinically meaningful impact on KW-6356 or M6 exposure.
引用
收藏
页码:549 / 559
页数:11
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