Wire Mary B, Ballow Charles H, Borland Julie, Shelton Mark J, Lou Yu, Yuen Geoffrey, Lin Jiang, Lewis Eric W
Clinical Pharmacology and Discovery Medicine, GlaxoSmithKline, Research Triangle Park, NC 27709, USA.
Antimicrob Agents Chemother. 2007 Aug;51(8):2982-4. doi: 10.1128/AAC.00008-07. Epub 2007 May 21.
Plasma ketoconazole (KETO), amprenavir (APV), and ritonavir (RTV) pharmacokinetics were evaluated in 15 healthy subjects after being treated with KETO at 200 mg once daily (QD), fosamprenavir (FPV)/RTV at 700/100 mg twice daily (BID), and then KETO at 200 mg QD plus FPV/RTV at 700/100 mg BID in this open-label study. The KETO area under the concentration-time curve at steady state was increased 2.69-fold with FPV/RTV. APV exposure was unchanged, and RTV exposure was slightly increased.
在这项开放标签研究中,对15名健康受试者进行了血浆酮康唑(KETO)、安普那韦(APV)和利托那韦(RTV)的药代动力学评估。受试者先接受每日一次200毫克的酮康唑治疗,然后接受每日两次700/100毫克的福沙普那韦(FPV)/利托那韦治疗,最后接受每日一次200毫克的酮康唑加每日两次700/100毫克的福沙普那韦/利托那韦治疗。与福沙普那韦/利托那韦联用时,稳态下酮康唑的浓度-时间曲线下面积增加了2.69倍。安普那韦的暴露量未改变,利托那韦的暴露量略有增加。