-
Views
-
Cite
Cite
Akil Jackson, Andrew Hill, Rebekah Puls, Laura Else, Janaki Amin, David Back, Enmoore Lin, Saye Khoo, Sean Emery, Roland Morley, Brian Gazzard, Marta Boffito, Pharmacokinetics of plasma lopinavir/ritonavir following the administration of 400/100 mg, 200/150 mg and 200/50 mg twice daily in HIV-negative volunteers, Journal of Antimicrobial Chemotherapy, Volume 66, Issue 3, March 2011, Pages 635–640, https://doi.org/10.1093/jac/dkq468
Close - Share Icon Share
Abstract
Data suggest that some licensed antiretroviral doses could be reduced. We assessed the safety, tolerability and pharmacokinetics of lopinavir/ritonavir at doses of 400/100, 200/150 and 200/50 mg twice daily in HIV-negative volunteers (http://clinicaltrials.gov/ct2/show/NCT00985543).
Male and female volunteers were administered lopinavir/ritonavir at doses of 400/100 mg (two lopinavir/ritonavir Meltrex 200/50 mg tablets, Regimen 1), 200/150 mg (one Meltrex tablet, one 100 mg ritonavir capsule, Regimen 2) and 200/50 mg (one Meltrex tablet, Regimen 3). Each dose was given twice daily for 7 days sequentially, separated by a 7 day wash-out period. Lopinavir/ritonavir steady-state pharmacokinetics was assessed over 12 h at the end of each phase (days 7, 21 and 35). Pharmacokinetic parameters were compared using the 400/100 mg twice daily dose as reference, by determining geometric mean ratios (GMRs) and 90% confidence intervals.
Twenty-two subjects (eight females) completed the study. Lopinavir AUC0–12 (ng h/mL), Cmax (ng/mL) and the minimum concentration (Ctrough) (ng/mL) for the 400/100, 200/150 and 200/50 mg twice daily doses, respectively, were as follows: 99 599, 73 603 and 45 146; 11 965, 8939 and 6404; and 5776, 4293 and 1749. Lopinavir pharmacokinetic parameters were significantly lower for Regimens 2 and 3: GMR (90% CI) AUC0–12, 0.74 (0.65–0.84) and 0.45 (0.40–0.51); Cmax, 0.75 (0.66–0.85) and 0.54 (0.40–0.60); and Ctrough, 0.74 (0.62–0.89) and 0.30 (0.25–0.36), respectively. All subjects taking the 400/100 and 200/150 mg twice daily doses, and 19 (86%) subjects taking 200/50 mg twice daily had lopinavir concentrations above the suggested minimum effective concentration of 1000 ng/mL.
These pharmacokinetic data show that therapeutic plasma concentrations of lopinavir can be achieved with 200/150 mg of lopinavir/ritonavir twice daily (one Meltrex tablet and one 100 mg ritonavir capsule twice daily).
