TY - JOUR
T1 - Effect of posaconazole on the pharmacokinetics of fosamprenavir and vice versa in healthy volunteers
AU - Brüggemann, Roger J.M.
AU - van luin, Matthijs
AU - Colbers, Engelina P.H.
AU - van den dungen, Myrthe W.
AU - Pharo, Cristina
AU - Schouwenberg, Bas J.J.W.
AU - Burger, David M.
N1 - Funding Information:
This work was supported by a research grant from GlaxoSmithKline.
PY - 2010/7/28
Y1 - 2010/7/28
N2 - Objectives: To manage the interaction between fosamprenavir/ritonavir and posaconazole, we hypothesized that ritonavir can be replaced by posaconazole as an alternative booster of fosamprenavir with no significant influence on posaconazole pharmacokinetics. Methods: This was an open-label, randomized, three period, cross-over, single-centre trial in 24 healthy volunteers. All subjects received the following three treatments for 10 days, separated by washout periods of 17 days: posaconazole 400 mg twice daily; fosamprenavir/ritonavir 700/100 mg twice daily; posaconazole 400 mg twice daily with fosamprenavir 700 mg twice daily. Results: Twenty subjects completed the trial. Geometric mean ratios (GMR; +90% confidence interval) of posaconazole AUC and Cmax when taken with fosamprenavir versus posaconazole alone were 0.77 (0.68-0.87) and 0.79 (0.71-0.89), respectively. The GMRs of amprenavir AUC and Cmax when taken as fosamprenavir and posaconazole versus fosamprenavir/ritonavir were 0.35 (0.32-0.39) and 0.64 (0.55-0.76), respectively. No serious adverse events were reported during the trial. Conclusion: Unboosted fosamprenavir should not be used concomitantly with posaconazole.
AB - Objectives: To manage the interaction between fosamprenavir/ritonavir and posaconazole, we hypothesized that ritonavir can be replaced by posaconazole as an alternative booster of fosamprenavir with no significant influence on posaconazole pharmacokinetics. Methods: This was an open-label, randomized, three period, cross-over, single-centre trial in 24 healthy volunteers. All subjects received the following three treatments for 10 days, separated by washout periods of 17 days: posaconazole 400 mg twice daily; fosamprenavir/ritonavir 700/100 mg twice daily; posaconazole 400 mg twice daily with fosamprenavir 700 mg twice daily. Results: Twenty subjects completed the trial. Geometric mean ratios (GMR; +90% confidence interval) of posaconazole AUC and Cmax when taken with fosamprenavir versus posaconazole alone were 0.77 (0.68-0.87) and 0.79 (0.71-0.89), respectively. The GMRs of amprenavir AUC and Cmax when taken as fosamprenavir and posaconazole versus fosamprenavir/ritonavir were 0.35 (0.32-0.39) and 0.64 (0.55-0.76), respectively. No serious adverse events were reported during the trial. Conclusion: Unboosted fosamprenavir should not be used concomitantly with posaconazole.
KW - Antiretroviral drugs
KW - Azole antifungal drugs
KW - Drug-drug interaction
KW - Healthy volunteers
KW - Pharmacokinetic
UR - http://www.scopus.com/inward/record.url?scp=77957226579&partnerID=8YFLogxK
U2 - 10.1093/jac/dkq280
DO - 10.1093/jac/dkq280
M3 - Article
C2 - 20667889
AN - SCOPUS:77957226579
SN - 0305-7453
VL - 65
SP - 2188
EP - 2194
JO - Journal of Antimicrobial Chemotherapy
JF - Journal of Antimicrobial Chemotherapy
IS - 10
M1 - dkq280
ER -