CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 299 enrolled
Drug / intervention
Valganciclovir CMV Prophylaxis +2 moredrug
Likely dose
Valganciclovir CMV Prophylaxis 900 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00372229
NCT00372229Phase 3Completed

A Randomized Trial Comparing Valcyte CMV Prophylaxis Versus Pre-emptive Therapy After Renal Transplantation Using Proteomics for Monitoring of Graft Alteration

Hoffmann-La Roche·interventional·Posted Sep 6, 2006·Updated Mar 11, 2020

In Brief

A Phase 3 clinical trial evaluating Valganciclovir CMV Prophylaxis, Valganciclovir (Pre-emptive CMV Therapy), and 1 other intervention for Cytomegalovirus Infections. Completed, enrolled 299 participants across 24 sites in 2 countries.

Detailed 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.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustria, Germany
Collaborators--

Timeline

Phase 3CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedSep 6, 2006
Enrollment StartMay 1, 2006
Primary CompletionOct 1, 2015
TodayJul 2, 2026
Enrollment to primary: 9.4 yearsPosted 19.8 years ago

Interventions

Valganciclovir CMV Prophylaxisdrug

900 mg valganciclovir, taken orally once daily, adjusted to renal function starting within 14 days of transplantation until Day 100 after transplantation.

Valganciclovir (Pre-emptive CMV Therapy)drug

If plasma polymerase chain reaction (PCR) ≥ 400 CMV copies/millilitre, then 1800 mg valganciclovir per day adjusted to renal function for at least 14 days until the second negative PCR (below 400 copies/ml) followed by secondary prophylaxis for 28 days with 900 mg valganciclovir adjusted to renal function. If CMV disease or no response to valganciclovir treatment after 14 days (not falling viral load), then intravenous (IV) ganciclovir or additional appropriate therapy could have been administered according to the local site's standard, instead of valganciclovir.

Ganciclovirdrug

If CMV disease or no response to valganciclovir treatment after 14 days (not falling viral load), then intravenous (IV) ganciclovir or additional appropriate therapy could have been administered according to the local site's standard, instead of valganciclovir.