drugset / Trial / NCT00431353

VICTOR Study - A Study of Valcyte (Valganciclovir po) Compared to Ganciclovir iv in Patients With Cytomegalovirus (CMV) Disease Who Are Solid Organ Transplant Recipients

NCT00431353

Phase 4 Completed 325 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelTreatment

Summary

This 2 arm study will evaluate the efficacy and safety of oral Valcyte compared with intravenous ganciclovir for the treatment of CMV disease in solid organ transplant recipients. Eligible patients will be randomized to receive either 1)Valcyte 900mg po bid or 2)ganciclovir 5mg/kg iv bid. The anticipated time on study treatment is 1-2 years and the target sample size is 100-500 individuals.

Timeline

Start
2004-04
Primary completion
2008-08
Completion
2008-08

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Ganciclovir Small molecule 5 mg/kg Intravenous
Subject Valganciclovir Small molecule 900 mg Oral