Coadministration of esomeprazole with fosamprenavir has no impact on steady-state plasma amprenavir pharmacokinetics

被引:0
作者
Shelton, MJ
Ford, SL
Borland, J
Lou, Y
Wire, MB
Min, SS
Xtie, ZG
Yuen, G
机构
[1] GlaxoSmithKline, Clin Pharmacol & Discovery Med, Res Triangle Pk, NC 27709 USA
[2] GlaxoSmithKline, Expt Pharmacogenet Discovery & Pipeline Genet, Res Triangle Pk, NC 27709 USA
关键词
fosamprenavir; amprenavir; esomeprazole; ritonavir; steady-state; pharmacokinetics;
D O I
暂无
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Objectives: To evaluate the drug interaction between fosamprenavir (FPV) and esomeprazole (ESO) after repeated doses in healthy adults. Methods: Subjects received ESO 20 mg once daily (qd) for 7 days followed by either ESO 20 mg qd + FPV 1400 mg twice daily (bid) or ESO 20 mg qd + FPV 700 mg bid + ritonavir (RTV) 100 mg bid for 14 days in arms 1 and 2, respectively. After a 21- to 28-day washout, subjects received either FPV 1400 mg bid for 14 days (arm 1) or FPV 700 mg bid + RTV 100 mg bid for 14 days (arm 2). Pharmacokinetic sampling was conducted on the last day of each treatment. Results: Simultaneous coadministration of ESO 20 mg qd with either FPV 1400 mg bid or FPV 700 mg bid + RTV 100 mg bid had no effect on steady-state amprenavir pharmacokinetics. The only effect on plasma ESO exposure was a 55% increase in area under the plasma concentration-time curve during a dosing interval, tau[AUC((0-tau))], after coadministration of ESO 20 mg qd with FPV 1400 mg bid. Conclusions: FPV 1400 mg bid or FPV 700 mg bid + RTV 100 mg bid may be coadministered simultaneously with ESO without dose adjustment. However, the impact of staggered administration of proton pump inhibitors (PPI) on plasma amprenavir exposure is unknown at present.
引用
收藏
页码:61 / 67
页数:7
相关论文
共 26 条
[1]  
AGARWALA S, 2005, 6 INT WORKSH CLIN PH
[2]  
AGARWALA S, 2005, 1I C RETR OPP INF 20
[3]   Pharmacokinetics, metabolism and interactions of acid pump inhibitors - Focus on omeprazole, lansoprazole and pantoprazole [J].
Andersson, T .
CLINICAL PHARMACOKINETICS, 1996, 31 (01) :9-28
[4]   Pharmacokinetics and pharmacodynamics of esomeprazole, the S-isomer of omeprazole [J].
Andersson, T ;
Röhss, K ;
Bredberg, E ;
Hassan-Alin, M .
ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2001, 15 (10) :1563-1569
[5]   Pharmacokinetic studies with esomeprazole, the (S)-isomer of omeprazole [J].
Andersson, T ;
Hassan-Alin, M ;
Hasselgren, G ;
Röhss, K ;
Weidolf, L .
CLINICAL PHARMACOKINETICS, 2001, 40 (06) :411-426
[6]   The comparative effects of lansoprazole, omeprazole, and ranitidine in suppressing gastric acid secretion [J].
Blum, RA ;
Shi, H ;
Karol, MD ;
GreskiRose, PA ;
Hunt, RH .
CLINICAL THERAPEUTICS, 1997, 19 (05) :1013-1023
[7]   Inhibition of the sulfoxidation of omeprazole by ketoconazole in poor and extensive metabolizers of S-mephenytoin [J].
Bottiger, Y ;
Tybring, G ;
Gotharson, E ;
Bertilsson, L .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1997, 62 (04) :384-391
[8]  
DEJESUS E, 2004, 44 INT C ANT AG CHEM
[9]   Clinical significance of the cytochrome P4502C19 genetic polymorphism [J].
Desta, Z ;
Zhao, XJ ;
Shin, JG ;
Flockhart, DA .
CLINICAL PHARMACOKINETICS, 2002, 41 (12) :913-958
[10]  
ELSTON RC, 2004, 15 INT AIDS C BANGK