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Completed Phase 3 Interventional Results available

Extension of Letermovir (LET) From Day 100 to Day 200 Post-transplant for the Prevention of Cytomegalovirus (CMV) Infection in Hematopoietic Stem Cell Transplant (HSCT) Participants (MK-8228-040)

ClinicalTrials.gov ID: NCT03930615

Public ClinicalTrials.gov record NCT03930615. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced May 20, 2026, 11:44 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Randomized, Double-blind, Placebo-controlled Clinical Trial to Evaluate the Safety and Efficacy of Letermovir (LET) Prophylaxis When Extended From 100 Days to 200 Days Post-transplant in Cytomegalovirus (CMV) Seropositive Recipients (R+) of an Allogenic Hematopoietic Stem Cell Transplant (HSCT)

Study identification

NCT ID
NCT03930615
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
220 participants

Conditions and interventions

Interventions

  • Letermovir Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 20, 2019
Primary completion
Oct 26, 2021
Completion
Mar 15, 2022
Last update posted
Aug 21, 2024

2019 – 2022

United States locations

U.S. sites
10
U.S. states
9
U.S. cities
10
Facility City State ZIP Site status
City of Hope National Medical Center ( Site 0158) Duarte California 91010
University of California Davis Medical Center ( Site 0156) Sacramento California 95817
University of Miami, Sylvester Comprehensive Cancer Center ( Site 0160) Miami Florida 33136
Indiana Blood and Marrow Transplantation ( Site 0175) Indianapolis Indiana 46237
Brigham & Women's Hospital ( Site 0161) Boston Massachusetts 02115
John Theurer Cancer Center at Hackensack University Med Ctr ( Site 0174) Hackensack New Jersey 07601
Memorial Sloan Kettering Cancer Center ( Site 0164) New York New York 10065
Duke University Medical Center ( Site 0169) Durham North Carolina 27710
The University of Texas MD Anderson Cancer Center ( Site 0154) Houston Texas 77030
Fred Hutchinson Cancer Research Center ( Site 0152) Seattle Washington 98109

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 22 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03930615, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 21, 2024 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03930615 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →