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Terminated Phase 2 Interventional Results available

Belatacept in Liver Transplant Recipients

ClinicalTrials.gov ID: NCT00555321

Public ClinicalTrials.gov record NCT00555321. 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 Jul 21, 2026, 5:31 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

Evaluation of Belatacept as First Line Immunosuppression in De Novo Liver Transplant Recipients

Study identification

NCT ID
NCT00555321
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
260 participants

Conditions and interventions

Interventions

  • Tacrolimus Drug
  • Basiliximab Drug
  • Belatacept More Intensive (MI) Drug
  • Belatacept Less Intensive (LI) Drug
  • Mycophenolate Mofetil (MMF) Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
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
Dec 31, 2007
Primary completion
Feb 28, 2010
Completion
May 31, 2011
Last update posted
Oct 17, 2012

2008 – 2011

United States locations

U.S. sites
19
U.S. states
16
U.S. cities
19
Facility City State ZIP Site status
Mayo Clinic Hospital Phoenix Arizona 85054
Usc University Hospital Los Angeles California 90033
University Of California San Francisco Medical Center San Francisco California 94143
Mayo Clinic Transplant Department Jacksonville Florida 32224
Lifelink Healthcare Institute Tampa Florida 33606
Emory University Hospital Atlanta Georgia 30322
Northwestern University Feinberg School Of Medicine Chicago Illinois 60611
Tulane Center For Abdominal Transplant New Orleans Louisiana 70112
Henry Ford Hospital Detriot Michigan 48202
University Of Minnesota Minneapolis Minnesota 55455
Washington University School Of Medicine St Louis Missouri 63110
Nyu School Of Medicine New York New York 10016
Westchester Medical Center Valhalla New York 10595
Carolinas Medical Center Charlotte North Carolina 28203
Univ. Of Cin. Coll. Of Med. Cincinnati Ohio 45267
Integris-Baptist Medical Ctr. Oklahoma City Oklahoma 73112
Hospital Of The University Of Pennsylvania Philadelphia Pennsylvania 19104
Baylor University Medical Center Dallas Texas 75246
Froedtert Memorial Lutheran Hospital 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 23 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00555321, 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 17, 2012 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00555321 live on ClinicalTrials.gov.

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