drugset / Trial / NCT02137772

Letermovir (MK-8228) Versus Placebo in the Prevention of Clinically-Significant Cytomegalovirus (CMV) Infection in Adult, CMV-Seropositive Allogeneic Hematopoietic Stem Cell Transplant Recipients (MK-8228-001)

NCT02137772 ↗

Phase 3 Completed 570 enrolled Merck Sharp & Dohme LLC
RandomizedParallel-groupDouble-blindPrevention

Summary

The study evaluated the efficacy and safety of letermovir (MK-8228) for the prevention of clinically-significant CMV infection in adult, CMV-seropositive recipients of allogeneic hematopoietic stem cell transplant (HSCT). The hypothesis being tested was that MK-8228 is superior to placebo in the prevention of clinically-significant CMV infection through Week 24 post-transplant.

Timeline

Start
2014-06-06
Primary completion
2016-08-08
Completion
2016-11-21

Outcome

Met primary endpoint

registry analysis (unspecified test); Letermovir vs Placebo; p <0.0001; Risk Difference (RD) -23.5 (95% CI -32.5 to -14.6); NCT02137772 ↗

paper Letermovir prophylaxis resulted in a significantly lower risk of clinically significant CMV infection than placebo. PMID 29211658 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Letermovir Small molecule 240 mg Oral
Subject Letermovir Small molecule 480 mg Oral