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Completed Phase 3 Interventional Results available

A Study to Evaluate a Therapeutic Vaccine, ASP0113, in Cytomegalovirus (CMV)-Seropositive Recipients Undergoing Allogeneic, Hematopoietic Cell Transplant (HCT)

ClinicalTrials.gov ID: NCT01877655

Public ClinicalTrials.gov record NCT01877655. 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 Jun 26, 2026, 6:30 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 Randomized, Double-Blind, Placebo-Controlled, Phase 3 Trial to Evaluate the Protective Efficacy and Safety of a Therapeutic Vaccine, ASP0113, in Cytomegalovirus (CMV)-Seropositive Recipients Undergoing Allogeneic, Hematopoietic Cell Transplant (HCT)

Study identification

NCT ID
NCT01877655
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Astellas Pharma Global Development, Inc.
Industry
Enrollment
514 participants

Conditions and interventions

Interventions

  • ASP0113 Biological
  • Placebo Drug

Biological · 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
Sep 10, 2013
Primary completion
Sep 27, 2017
Completion
Feb 28, 2022
Last update posted
Oct 23, 2024

2013 – 2022

United States locations

U.S. sites
27
U.S. states
22
U.S. cities
25
Facility City State ZIP Site status
Site US10028 Birmingham Alabama 35294
Site US10044 Tucson Arizona 85724
Site US10035 San Francisco California 94143
Site US10026 Stanford California 94305
Site US10030 Tampa Florida 33612
Site US10012 Atlanta Georgia 30322
Site US10013 Chicago Illinois 60612
Site US10007 Indianapolis Indiana 46237
Site US10020 Westwood Kansas 66205
Site US10010 Louisville Kentucky 40202
Site US10043 Baltimore Maryland 21201
Site US10011 Baltimore Maryland 21205
Site US10021 Boston Massachusetts 02114
Site US10036 Rochester Minnesota 55905
Site US10042 St Louis Missouri 63110
Site US10023 Hackensack New Jersey 07601-2105
Site US10047 New York New York 10032
Site US10027 Rochester New York 14642
Site US10025 Chapel Hill North Carolina 27514
Site US10016 Nashville Tennessee 37232
Site US10002 Dallas Texas 75246
Site US10045 Houston Texas 77030
Site US10046 Salt Lake City Utah 84143
Site US10031 Richmond Virginia 23298
Site US10039 Seattle Washington 98108
Site US10024 Seattle Washington 98109
Site US10019 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 56 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01877655, 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 Oct 23, 2024 · Synced Jun 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01877655 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →