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Clinical Trial
. 2003 Sep;47(9):2788-95.
doi: 10.1128/AAC.47.9.2788-2795.2003.

Pharmacokinetics, safety, and tolerability of oral posaconazole administered in single and multiple doses in healthy adults

Affiliations
Clinical Trial

Pharmacokinetics, safety, and tolerability of oral posaconazole administered in single and multiple doses in healthy adults

Rachel Courtney et al. Antimicrob Agents Chemother. 2003 Sep.

Abstract

The pharmacokinetics, safety, and tolerability of posaconazole, an investigational triazole antifungal, were evaluated following the administration of rising single and multiple oral doses. A total of 103 healthy adults were enrolled in two phase I trials. Each study had a double-blind, placebo-controlled, parallel-group design with a rising single-dose (RSD) or rising multiple-dose (RMD) scheme. In the RSD study, subjects received single doses of posaconazole oral tablets (50 to 1200 mg) or placebo. In the RMD study, subjects received posaconazole oral tablets (50 to 400 mg) or placebo twice daily for 14 days. By using model-independent methods, the area under the plasma concentration-time curve and the maximum concentration in plasma were determined and used to assess dose proportionality. In the RSD study, the levels of posaconazole in plasma increased proportionally between the 50- and 800-mg dose range, with saturation of absorption occurring above 800 mg. Dose proportionality was also observed in the RMD study. In both studies, the apparent volume of distribution was large (range, 343 to 1341 liters) and the terminal-phase half-life was long (range, 25 to 31 h). Posaconazole was well tolerated at all dose levels, and the adverse events were not dose dependent. No clinically significant changes in clinical laboratory test values or electrocardiograms were observed. Following the administration of single and twice-daily rising doses, the level of posaconazole exposure increased in a dose-proportional manner. The long elimination-phase half-life of posaconazole supports once- or twice-daily dosing in clinical trials; however, additional studies are required to determine if further division of the dose will enhance exposure.

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Figures

FIG. 1.
FIG. 1.
Chemical structure of posaconazole. Me, methyl.
FIG. 2.
FIG. 2.
Mean concentrations of posaconazole in plasma over time after administration of a single dose.
FIG. 3.
FIG. 3.
Mean concentrations of posaconazole (multiple doses) in plasma by dose on day 1 of twice-daily administration.
FIG. 4.
FIG. 4.
Mean concentration of posaconazole in plasma by dose on day 14 of twice-daily administration.
FIG. 5.
FIG. 5.
Mean concentrations of posaconazole in plasma after twice-daily administration over the 14-day study period.

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