drugset / Trial / NCT07235683

Combination Letermovir and Standard of Care Antiviral for Enhanced Antiviral Response in Cytomegalovirus Infection in Lung Transplant Recipients

NCT07235683

Phase 4 Recruiting 40 enrolled University Health Network, Toronto
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of the CLEAR-CMV trial is to evaluate the efficacy of letermovir therapy plus standard of care (SOC) antiviral compared to SOC plus placebo in achieving clearance of CMV viremia by week 3 in lung transplant recipients with active CMV infection.

Timeline

Start
2025-12-24
Primary completion
2027-08
Completion
2027-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Letermovir Small molecule 480 mg Oral
Background Ganciclovir Small molecule
Background Valganciclovir Small molecule