You can install PPMD to make it easier to access on your device. A network connection is still required to view medication and interaction information.
You should now see a icon on your home screen.
Tap then menu button, and then tap Install.
Not all web browsers and platforms support progressive web applications (PWA). Consult the documentation for your web browser for additional assistance.
N/A
Two single sequence studies were conducted to assessthe effectof multiple-dose BMS-650032 (asunaprevir) on the pharmacokinetics (PK) ofa cocktail of cytochrome P (CYP) -450 probes and a P-glycoprotein (P-gp) probe. The study subjects includedhealthy men and women ages 18 to 49 years with a BMI of 18 to 32kg/m2.In studyAI447020 on Days 1 and 11, 19 subjects receivedsingle oral doses of substrates of CYP1A2 (Caffeine 200mg), CYP2D6 (Dextromethorphan30mg), CYP3A4 (Midazolam 5mg), CYP2C9 (Losartan25mg), and CYP2C19 (Omeprazole 40mg) concurrently. On days 2-11, 200mg BID of asunaprevir was given. Blood sampleswere collected for PK analysis through 24h post-dose on Days 1 and 11 for the probe substrates. The geometric mean ratios (GMR) and 90% confidence intervals (90%CI) were calculated to show the magnitude of change during co-administration.
Drug NameCmaxGMR (90% CI)AUC GMR (90% CI)Omeprazole0.957 (0.790, 1.160)0.804 (0.691, 0.936)Co-administration of asunaprevir and omeprazole showed a small change in the Cmaxand AUC of omeprazole. Asunaprevir decreased the Cmaxand AUC of omeprazole by 4% and 20%, respectively. Based on the results of this study, it would appear that there are no clinically signficiant changes in the Cmaxor AUC of omeprazole when co-administered with asunaprevir.
T Eley, D Gardiner, A Persson, et al. Evaluation of drug interaction potential of the hcv protease inhibitor bms-650032 at 200mg twice daily (bid) in metabolic cocktail and p-glycoprotein (p-gp) probe studies in healthy volunteers. 62nd Annual Meeting Of The American Association For The Study Of Liver Diseases. San Francisco, CA. ; 2011.