NCT00175994

Bioavailability and Metabolism of Voriconazole in Relation to Its Modulation by the CYP2C19 Genetic Polymorphism

Bioavailability and Metabolism of Voriconazole as a Function of the CYP2C19 Genotype

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 24 (planned)
• Sponsor: Heidelberg University · Academic / Other
• Sex: All
• Age: 18 Years – 50 Years
• Healthy volunteers: Accepted

Summary

The purposes of this study are: * To determine the absolute bioavailability of voriconazole after a single oral dose (400 mg voriconazole \[VFEND brand\]) in comparison to intravenous (i.v.) administration (400 mg VFEND, equivalent to two 10 mg/ml-infusates, each containing 200 mg voriconazole \[VRC\]) in healthy individuals stratified according to the three predominant CYP2C19 genotypes * To investigate the possible pathways of metabolism and their modulation according to genetic polymorphism of CYP2C19 after i.v. and oral administration of VRC.

Detailed description

As CYPs are mainly involved in VRC metabolism it is likely that also gut wall metabolism by CYPs occurs. However, no substantial first pass metabolism of VRC has been reported. In humans the VRC metabolism has not been studied systematically. It is therefore important to assess VRC metabolism on its own and in addition the influence of CYP2C19 genetic polymorphisms on the formation of the different VRC metabolites.

Conditions

• Healthy

Timeline

• Start date: 2005-07-01
• Completion: 2006-07-01
• First posted: 2005-09-15
• Last updated: 2007-04-17

Locations

1 site across 1 country: Germany