drugset / Trial / NCT01552369

CMV Antiviral Prevention Strategies in D+R-Liver Transplants ("CAPSIL")

NCT01552369 ↗

RandomizedParallel-groupOpen-labelTreatment

Summary

This is a trial of preemptive therapy vs. prophylaxis for prevention of Cytomegalovirus (CMV) disease in R-D+ liver transplant patients. Subjects will be randomized within 10 days of transplant to receive in an open label design, either antiviral prophylaxis with valganciclovir, 900 mg orally once daily or preemptive therapy (weekly monitoring for CMV viremia by plasma PCR) for 100 days post-randomization with initiation of oral valganciclovir 900mg orally twice daily at onset of CMV viremia and continued until plasma PCR is negative on two consecutive weekly PCR tests). A minimum of 176 subjects will be enrolled in the study. The study duration is 7 years. The primary objective of this study is to compare prophylaxis versus preemptive therapy using valganciclovir for the prevention of CMV disease in R-/D+ liver transplant recipients.

Timeline

Start
2012-10-29
Primary completion
2018-06-22
Completion
2018-06-22

Outcome

Met primary endpoint

paper The incidence of CMV disease was significantly lower with preemptive therapy than antiviral prophylaxis PMID 32286644 ↗

registry analysis (superiority test); Preemptive Therapy vs Prophylaxis; p = 0.0396; Mantel Haenszel NCT01552369 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Valganciclovir Small molecule 900 mg Oral