The effect of fluconazole on the pharmacokinetics of rosuvastatin

Objective: To examine the effect of fluconazole, a potent inhibitor of CYP2C9 and CYP2C19, on the pharmacokinetics of rosuvastatin in healthy volunteers. Significantly increased plasma concentrations of fluvastatin have been observed following co-administration with fluconazole. Methods: This was a randomised, double-blind, two-way crossover, placebo-controlled trial. Healthy male volunteers (n=14) were given fluconazole 200 mg or matching placebo once daily for 11 days; rosuvastatin 80 mg was co-administered on day 8 of dosing. Plasma concentrations of rosuvastatin, N-desmethyl rosuvastatin, and active and total 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase inhibitors were measured up to 96 h post-dose. Results: Following co-administration with fluconazole, rosuvastatin geometric least-square mean area under the plasma concentration-time curve (AUC 0-1 ) and peak plasma concentration (C max ) were increased by 14% and 9%, respectively, compared with placebo (90% confidence intervals for the treatment ratios: 0.967 to 1.341 and 0.874 to 1.355, respectively). Individual treatment ratios for AUC 0-t ranged from 0.59 to 2.23, and for C max ranged from 0.52 to 2.28. The limited data available for the N-desmethyl metabolite show that geometric mean C max was decreased by approximately 25% compared with placebo. Rosuvastatin accounted for essentially all of the circulating active HMG--CoA reductase inhibitors and most (> 90%) of the total inhibitors. Fluconazole did not affect the proportion of circulating active or total inhibitors accounted for by circulating rosuvastatin. Conclusions: Fluconazole produced only small increases in rosuvastatin AUC 0-t and C max , which were not considered to be of clinical relevance. The results support previous in-vitro findings that CYP2C9 and CYP2C19 metabolism is not an important clearance mechanism for rosuvastatin.