Solid Drug Development Geneva, Switzerland.
Covance Clinical Research Unit (CRU) Basel, Switzerland.
Pharmacol Res Perspect. 2014 Feb;2(1):e00020. doi: 10.1002/prp2.20. Epub 2014 Jan 26.
The aim of the study is to evaluate the safety, tolerability and pharmacokinetics (PK) of the JNK inhibitor XG-102 in a randomized, double blind, placebo controlled, sequential ascending dose parallel group Phase 1 Study. Three groups of male subjects received as randomly assigned ascending single XG-102 doses (10, 40, and 80 μg/kg; 6 subjects per dose) or placebo (2 subjects per dose) as an intravenous (IV) infusion over 60 min. Safety and tolerability were assessed by physical examination, vital signs, electrocardiography, eye examination, clinical laboratory tests and adverse events (AEs). PK was analyzed using noncompartmental methods. All reported AEs were mild to moderate and neither their number nor their distribution by System Organ Class suggest a dose relationship. Only headache and fatigue were considered probably or possibly study drug related. Headache frequency was similar for active and placebo, consequently this was not considered to be drug related but probably to study conditions. The other examinations did not show clinically relevant deviations or trends suggesting a XG-102 relationship. Geometric mean half-life was similar among doses, ranging from 0.36 to 0.65 h. Geometric mean XG-102 AUC0-last increased more than linearly with dose, 90% confidence intervals (CIs) did not overlap for the two highest doses. Geometric mean dose normalized C max values suggest a more than linear increase with dose but 90% CIs overlap. It may be concluded that XG-102 single IV doses of 10-80 μg/kg administered over 1 h to healthy male subjects were safe and well tolerated.
本研究旨在评估 JNK 抑制剂 XG-102 的安全性、耐受性和药代动力学(PK),采用随机、双盲、安慰剂对照、序贯递增剂量平行组的 1 期研究。三组男性受试者分别接受随机递增的单剂 XG-102 静脉输注(6 名受试者/剂量,60 分钟)或安慰剂(2 名受试者/剂量)。安全性和耐受性通过体格检查、生命体征、心电图、眼科检查、临床实验室检查和不良事件(AE)进行评估。PK 采用非房室分析方法进行分析。所有报告的 AE 均为轻度至中度,其数量和系统器官类别分布均未提示与剂量有关。仅头痛和疲劳被认为可能与研究药物有关。活性药物和安慰剂的头痛频率相似,因此不认为与药物有关,而可能与研究条件有关。其他检查未显示临床相关偏差或趋势表明与 XG-102 有关。剂量间几何平均半衰期相似,范围为 0.36 至 0.65 小时。几何平均 XG-102 AUC0-last 随剂量呈非线性增加,最高两剂量的 90%置信区间(CI)不重叠。几何平均剂量归一化 Cmax 值提示剂量呈非线性增加,但 90%CI 重叠。可以得出结论,1 小时内静脉输注 10-80μg/kg 的 XG-102 单次剂量在健康男性受试者中是安全且耐受良好的。