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Clinical Trial Summary

Valacyclovir has replaced acyclovir in many clinical scenarios. Pharmacokinetic data support the use of oral valacyclovir in children, but practical problems exist in children having to take adult-dose tablets. A formulation with acceptable palatability, good pharmaceutical quality and possibility of flexible dosing is developed. Pharmacokinetic data of this formulation is missing. The present study investigates the pharmacokinetics of valacyclovir oral solution in children by determine the area under the curve (AUC0-12), time above critical concentration (Ccrit), Cmax and Tmax of acyclovir. Secondary, the safety profile of a single dose of valacyclovir oral solution will be determined.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04081480
Study type Interventional
Source Radboud University
Contact
Status Terminated
Phase N/A
Start date December 10, 2019
Completion date May 12, 2021

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