drugset / Trial / NCT00372229

A Study of Valcyte (Valganciclovir) CMV Prophylaxis After Renal Transplantation

NCT00372229

Phase 3 Completed 299 enrolled Hoffmann-La Roche
RandomizedParallel-groupOpen-labelPrevention

Summary

This 2 arm study will compare the efficacy of 100 days of Valcyte (900mg po daily) prophylaxis with that of no prophylaxis, under the condition of pre-emptive therapy of active CMV infection, in CMV positive renal transplant recipients. The influence of the two prevention concepts on the occurrence of direct and indirect effects of active CMV infections will be compared. The anticipated time on study treatment is 3 months-1 year, and the target sample size is 100-500 individuals.

Timeline

Start
2006-05
Primary completion
2015-10
Completion
2015-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Valganciclovir Small molecule 900 mg Oral
Subject Valganciclovir Small molecule 1800 mg Oral
Comparator Ganciclovir Small molecule Intravenous