Pharmacokinetics and safety of multiple-dose valaciclovir in geriatric volunteers with and without concomitant diuretic therapy

Abstract

A randomized, double-blind study was conducted to evaluate the safety and pharmacokinetics of acyclovir following multiple-dose oral administration of valaciclovir (three times a day for 8 days) in geriatric volunteers (65 to 83 years of age). Pharmacokinetic evaluation was performed for three groups: normotensive subjects given 500-mg doses of valaciclovir (n = 11), normotensive subjects given 1,000-mg doses of valaciclovir (n = 9), and thiazide diuretic-treated hypertensive subjects given 500-mg doses of valaciclovir (n = 9). Valaciclovir, the l-valyl ester of acyclovir, was rapidly absorbed and converted to acyclovir, with plasma valaciclovir concentrations generally undetectable or ≤0.4 μg/ml. The peak concentration of drug in plasma (C(max)) for acyclovir occurred at 1 to 2 h, and the half- life of acyclovir was 3 to 4 h in all three elderly groups. The C(max) and area under the concentration-time curve from 0 h to infinity (AUC(0-∞)) values of acyclovir obtained on days 1 and 8 indicated no unexpected accumulation at steady state. The steady-state acyclovir C(max) (4.30 and 5.98 μg/ml) and daily AUC(0-∞) (44 and 74 h · μg/ml) following dosing of valaciclovir (500 and 1,000 mg) three times a day were two to three times greater than those expected after high-dose oral acyclovir treatment (800 mg, five times daily). There were no valaciclovir-related changes or abnormalities in safety parameters and no reports of serious adverse experiences in these elderly volunteers. The plasma acyclovir concentration- time curves for the hypertensive and normotensive (500-mg valaciclovir treatment) elderly groups were almost superimposable, and acyclovir pharmacokinetic parameters for the two groups were not significantly different, indicating that concomitant thiazide diuretics do not alter acyclovir pharmacokinetics following valaciclovir dosing in the elderly. Compared with historical data for younger volunteers (creatinine clearance [CL(CR)] > 75 ml/min/1.73 m2), the elderly subjects (CL(CR) = 40 to 65 ml/min/1.73 m2) showed higher (~ 15 to 20%) mean C(max)s and higher (~ 30 to 50%) mean AUC(0-∞)s of acyclovir (P