Adkison Kimberly K, Gan Jianjun, Elko-Simms Lucinda, Gardner Stephen, Dumont Etienne, Jones Lori S, Saunders Joanne, Marbury Thomas, Smith William, Berg Jolene, Galloway Christopher, Stump Patrick J
GlaxoSmithKline, Research Triangle Park, NC, USA.
PPD, Morrisville, NC, USA.
J Clin Pharmacol. 2015 Sep;55(9):1042-50. doi: 10.1002/jcph.512. Epub 2015 May 25.
JNJ-56914845 (GSK2336805) is a hepatitis C virus nonstructural protein 5A inhibitor under development for the treatment of chronic hepatitis C (CHC) infection. This open-label, parallel-group, 2-part study evaluated the pharmacokinetics and safety of a single oral 60 mg dose of JNJ-56914845 in 4 cohorts: healthy, mild, moderate, and severe hepatic impairment (n = 8/cohort). Severity of hepatic impairment was categorized using Child-Pugh score, and the healthy subjects were matched for age, sex, body mass index, and smoking status to the moderate hepatic impairment cohort. JNJ-56914845 plasma AUC0-∞ was 26%, 52%, and 45% lower in subjects with mild, moderate, and severe hepatic impairment, respectively, relative to healthy subjects with no difference in half-life among the groups. The apparent oral clearance and volume of distribution were higher in subjects with hepatic impairment. The lower plasma concentrations were largely explained by decreased plasma protein binding in hepatically impaired subjects. One subject with severe hepatic impairment had 2 non-drug-related serious adverse events: an esophageal bleed requiring hospitalization, encephalopathy. Although hepatically impaired subjects have lower exposures than healthy matched controls, they had similar or slightly higher exposures than those observed in past studies of noncirrhotic, CHC patients, suggesting that no dose adjustments for hepatic impairment will be needed.
JNJ-56914845(GSK2336805)是一种正在研发用于治疗慢性丙型肝炎(CHC)感染的丙型肝炎病毒非结构蛋白5A抑制剂。这项开放标签、平行组、两部分的研究评估了4个队列中单次口服60毫克剂量JNJ-56914845的药代动力学和安全性:健康、轻度、中度和重度肝功能损害(每组n = 8)。肝功能损害的严重程度采用Child-Pugh评分进行分类,健康受试者在年龄、性别、体重指数和吸烟状况方面与中度肝功能损害队列相匹配。与健康受试者相比,轻度、中度和重度肝功能损害受试者的JNJ-56914845血浆AUC0-∞分别降低了26%、52%和45%,各组间半衰期无差异。肝功能损害受试者的表观口服清除率和分布容积较高。血浆浓度较低主要是由于肝功能受损受试者血浆蛋白结合减少所致。一名重度肝功能损害受试者发生了2起与药物无关的严重不良事件:一次需要住院治疗的食管出血、脑病。虽然肝功能受损受试者的暴露量低于健康匹配对照组,但与过去非肝硬化CHC患者研究中观察到的暴露量相似或略高,这表明无需针对肝功能损害进行剂量调整。