Safety, Tolerability and Pharmacokinetics of Single and Multiple Doses of Mirogabalin in Healthy Chinese Participants: A Randomized, Double-Blind, Placebo-Controlled Study

被引:4
|
作者
Li, Yi [1 ,2 ]
Toyama, Kaoru [3 ]
Nakatsu, Takafumi [3 ]
Ishizuka, Hitoshi [3 ]
Wu, Hailan [1 ,2 ]
Cao, Guoying [2 ,4 ]
Yu, Jicheng [2 ,4 ]
Wang, Yu [1 ,2 ]
Liu, Xiaofen [1 ,2 ]
Guo, Beining [1 ,2 ]
Wu, Jufang [1 ,2 ,4 ]
Yu, Peimin [5 ]
Hong, Zhen [5 ]
Zhang, Jing [1 ,2 ,4 ]
Wu, Xiaojie [2 ,4 ]
机构
[1] Fudan Univ, Huashan Hosp, Inst Antibiot, Shanghai, Peoples R China
[2] Natl Populat & Family Planning Commiss, Key Lab Clin Pharmacol Antibiot, Shanghai, Peoples R China
[3] Daiichi Sankyo Co Ltd, Shinagawa Ku, Tokyo, Japan
[4] Fudan Univ, Huashan Hosp, Phase Clin Res Ctr 1, 12 Wulumuqi Middle Rd, Shanghai 200040, Peoples R China
[5] Fudan Univ, Dept Neurol, Shanghai, Peoples R China
关键词
China; Neuropathic pain; Mirogabalin; Multiple-dose; Pharmacokinetics; Phase I; Post-herpetic neuralgia; Safety; Single-dose; Tolerability; PAINFUL DIABETIC-NEUROPATHY; HERPES-ZOSTER; SUBUNIT; IDENTIFICATION; PHARMACOLOGY; POPULATION; PREVALENCE; MANAGEMENT; EFFICACY;
D O I
10.1007/s12325-022-02424-7
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Introduction: Mirogabalin is a treatment option for patients with neuropathic pain; however, safety, tolerability, and pharmacokinetics (PK) data specifically for Chinese individuals are limited to a single-dose study. We aimed to assess these for both single- and multiple-dose mirogabalin in healthy Chinese participants. Methods: In this randomized, double-blind, placebo-controlled, phase I study, 54 healthy Chinese men and women aged 18-45 years were randomly allocated to receive single- (5, 10, or 15 mg, daily) or multiple-dose (5 mg titrated to 15 mg, twice-daily, over 22 days) oral mirogabalin or placebo. In each of three single-dose groups, 10 participants received mirogabalin and 2 received placebo; in the multiple-dose group, 14 participants received mirogabalin and 4 received placebo. The primary endpoints were PK, safety, and tolerability variables, including treatment-emergent adverse events (TEAEs), laboratory tests, and vital signs. PK data were collected for both single- and multiple-dose cohorts and evaluated by non-compartmental analysis. Results: Single- and multiple-dose mirogabalin was generally well tolerated with no deaths, serious TEAEs, or TEAEs leading to treatment discontinuation. Frequently reported TEAEs included dizziness, nystagmus, increased blood triglycerides, headache, and increased blood uric acid and creatine phosphokinase. Single-dose mirogabalin was rapidly absorbed (median time to maximum plasma concentration, 1.00 h) and eliminated (mean terminal elimination half-life, 2.57-3.08 h). The exposure was approximately dose-proportional. In the multiple-dose cohort, the trough plasma concentration increased dose-proportionally, and exposure and clearance were comparable to that following a single 15-mg dose. The mean cumulative amount excreted into urine up to 48 h post-dose increased in a dose-proportional manner, the mean cumulative percentage excreted into urine was 61.9%-74.3%, and renal clearance remained relatively constant. Conclusion: Consistent with previous phase I studies in other populations, mirogabalin was safe and well tolerated in healthy Chinese participants at single and multiple doses of up to 15 mg twice-daily.
引用
收藏
页码:1628 / 1643
页数:16
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