Nippon Boehringer Ingelheim Co Ltd, Kobe, Japan.
Nippon Boehringer Ingelheim Co Ltd, Tokyo, Japan.
Clin Ther. 2019 May;41(5):961-971. doi: 10.1016/j.clinthera.2019.03.014. Epub 2019 Apr 17.
This study's primary goal was to evaluate the safety profile, tolerability, pharmacokinetics, and dose proportionality of BI 425809, a potent and selective inhibitor of glycine transporter 1, in healthy Chinese and Japanese subjects.
This single center, double-blind, single-rising dose study conducted in Korea randomly assigned (3:1) subjects within each ethnic subgroup (Chinese and Japanese) to receive a single dose of BI 425809 (10, 25, or 50 mg) or placebo. The primary end point was number (%) of subjects with drug-related adverse events (AEs). Secondary end points included AUC, C, t, and t for BI 425809 in plasma. The CL/F and volume of distribution (V/F) were also measured.
Of the 49 subjects enrolled into the study (24 Chinese, 25 Japanese), 36 were randomly assigned to receive BI 425809 (12 per dose group) and 13 to receive placebo. All subjects were analyzed for the primary end point and completed the study. Overall, 4 of 49 subjects (8.2%) reported ≥1 AE (placebo: n = 1, BI 425809: n = 3). One drug-related AE of moderate somnolence was reported by a Japanese subject who received placebo. In both subgroups, slightly lower than dose-proportional increases in exposure (AUC and C) were observed with increasing dose. In addition, median t was 3.5-4.0 h, with a geometric mean t of 29.0-41.2 h. CL/F was similar between Chinese and Japanese subjects and increased with increasing dose (10-50 mg: 68.1-111 mL/min). V/F was 209-315 L and similar between the subgroups.
BI 425809 was generally well tolerated in healthy Chinese and Japanese subjects with no significant findings for tolerability. No apparent difference in the pharmacokinetic variables of BI 425809 was observed between Chinese and Japanese subjects. The safety profile results and pharmacokinetic exposure levels are consistent with previous trials in Caucasian subjects. ClinicalTrials.gov identifier: NCT02383888.
本研究的主要目的是评估 BI 425809(一种有效的甘氨酸转运体 1 抑制剂)在健康中国和日本受试者中的安全性概况、耐受性、药代动力学和剂量比例性。
这项在韩国进行的单中心、双盲、单次递增剂量研究,按种族亚组(中国和日本)以 3:1 的比例随机分配(n=49)受试者,接受单次 BI 425809(10、25 或 50mg)或安慰剂治疗。主要终点是药物相关不良事件(AE)的发生例数(%)。次要终点包括血浆中 BI 425809 的 AUC、C、t 和 t1/2。CL/F 和分布容积(V/F)也进行了测量。
在纳入的 49 名受试者中(中国受试者 24 名,日本受试者 25 名),36 名随机分配接受 BI 425809 治疗(每组 12 名),13 名接受安慰剂治疗。所有受试者均对主要终点进行了分析并完成了研究。总体而言,49 名受试者中有 4 名(8.2%)报告了≥1 例 AE(安慰剂:n=1,BI 425809:n=3)。一名接受安慰剂的日本受试者报告了 1 例与药物相关的中度嗜睡的 AE。在两个亚组中,随着剂量的增加,暴露量(AUC 和 C)略低于剂量比例增加。此外,中位 t1/2 为 3.5-4.0h,几何均数 t1/2 为 29.0-41.2h。CL/F 在中、日受试者之间相似,且随剂量增加而增加(10-50mg:68.1-111mL/min)。V/F 为 209-315L,且在两个亚组之间相似。
BI 425809 在健康的中国和日本受试者中总体耐受性良好,无明显的耐受性相关发现。在中、日受试者中,BI 425809 的药代动力学变量无明显差异。安全性概况结果和药代动力学暴露水平与之前在白种人受试者中的试验结果一致。临床试验注册号:NCT02383888。