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Completed Phase 3 Interventional Results available

A Study of Maribavir Compared to Valganciclovir to Treat Cytomegalovirus Infections in People Who Have Received Stem Cell Transplants

ClinicalTrials.gov ID: NCT02927067

Public ClinicalTrials.gov record NCT02927067. 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 Oct 30, 2026, 1:32 PM 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, Multicenter, Randomized, Double-blind, Double-dummy, Active-controlled Study to Assess the Efficacy and Safety of Maribavir Compared to Valganciclovir for the Treatment of Cytomegalovirus (CMV) Infection in Hematopoietic Stem Cell Transplant Recipients

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study is about treatment options for cytomegalovirus infections in people who have received stem cell transplants. The main aim of the study is to check if the cytomegalovirus infection can no longer be detected after treatment with marivabir or valganciclovir. Participants will take 2 tablets of marivabir or valganciclovir and 2 tablets of placebo twice a day for 8 weeks. A placebo will look like marivabir or valganciclovir but will not have any medicine in it. After treatment, each participant will be followed up for up to 12 weeks. Participants will visit their study clinic up to 18 times during the study.

Study identification

NCT ID
NCT02927067
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Shire
Industry
Enrollment
553 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
16 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
Apr 14, 2017 (Actual)
Primary completion
Jul 1, 2022 (Actual)
Completion
Jul 1, 2022 (Actual)
Last update posted
Mar 3, 2023

2017 – 2022

United States locations

U.S. sites
28
U.S. states
17
U.S. cities
23
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294 —
UCLA Medical Center Los Angeles California 90095 —
Stanford University Stanford California 94305 —
Colorado Blood Cancer Institute - PPDS Denver Colorado 80218 —
Yale University School of Medicine New Haven Connecticut 06520 —
Emory University Atlanta Georgia 30322 —
University of Chicago Chicago Illinois 60637 —
Loyola University Medical Center Maywood Illinois 60153 —
University of Maryland School of Medicine Baltimore Maryland 21201 —
Johns Hopkins Hospital Baltimore Maryland 21205 —
Beth Israel Deaconess Medical Center Boston Massachusetts 02115 —
Brigham and Womens Hospital Boston Massachusetts 02115 —
UMass Memorial Medical Center Worcester Massachusetts 01655 —
Harper University Hospital Detroit Michigan 48201 —
Henry Ford Health System Detroit Michigan 48202 —
University of Minnesota Minneapolis Minnesota 55454 —
Mayo Clinic - PIN Rochester Minnesota 59905 —
Hackensack University Medical Center Hackensack New Jersey 07601 —
Joan and sandford I. Weill Medical College of Cornell University Clinic New York New York 10021 —
Columbia University Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
University of Pennsylvania Philadelphia Pennsylvania 19104 —
TriStar Centennial Medical Center Nashville Tennessee 37203-1624 —
Saint Davids South Austin Medical Center Austin Texas 78704 —
University of Texas MD Anderson Cancer Center Houston Texas 77030 —
Texas Transplant Institute San Antonio Texas 78229 —
VA Puget Sound Health Care System - NAVREF - PPDS Seattle Washington 98108 —
The Medical College of Wisconsin, Inc. Milwaukee Wisconsin 53226 —

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 101 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02927067, 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 Mar 3, 2023 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02927067 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →