About this trial

The purpose of this study is to compare the safety and efficacy of letermovir with valganciclovir for prevention of Cytomegalovirus (CMV) viremia in moderate to high risk serostatus heart transplant recipients.

Eligibility criteria

Qualifiers

None

Disqualifiers

None

Trial design

Treatments tested in this trial

  • Letermovir
  • Valganciclovir

Treatment groups

150 Participants
are divided into 3 treatment groups

Locations

2
Columbia University/NYP Milstein Hospital10032, New YorkNew York, United States
NYP-Weill Cornell10021, New YorkNew York, United States

Sponsors and collaborators

Columbia University

Lead sponsor

Cornell University

Collaborator