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Completed Phase 2 Interventional Results available

Study Comparing the Safety and Efficacy of Belatacept With That of Cyclosporine in Patients With a Transplanted Kidney

ClinicalTrials.gov ID: NCT00035555

Public ClinicalTrials.gov record NCT00035555. 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 16, 2026, 10:21 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

Phase II/III, Open-Label, Randomized, Controlled, Multiple-Dose Study of Efficacy and Safety of BMS-224818 (Belatacept) as Part of a Quadruple Drug Regimen in First Renal Transplant Recipients

Brief summary

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

The purpose of this study is to determine whether treatment with Belatacept (BMS-224818) is as efficacious as treatment with cyclosporine at preventing acute rejection and with a superior safety/tolerability profile (better kidney function and blood pressure, fewer lipid problems, less diabetes mellitus).

Study identification

NCT ID
NCT00035555
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Bristol-Myers Squibb
Industry
Enrollment
230 participants

Conditions and interventions

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
Mar 2001 (Type not available)
Primary completion
Jan 2004 (Actual)
Completion
Jul 2012 (Actual)
Last update posted
Jan 13, 2014

2001 – 2012

United States locations

U.S. sites
12
U.S. states
12
U.S. cities
12
Facility City State ZIP Site status
Univ. of Calif. - San Francisco San Francisco California 94143-0001 —
Emory Univ. School of Medicine Atlanta Georgia 30322 —
Johns Hopkins University Baltimore Maryland 21205 —
Massachusetts General Hospital Boston Massachusetts 02114 —
Mayo Clinic Rochester Minnesota 55905 —
Univ. of Nebraska Medical Center Omaha Nebraska 68198-1002 —
Saint Barnabas Medical Center Livingston New Jersey 07039 —
Mount Sinai Medical Center New York New York 10029-6574 —
Univ. of Pennsylvania Philadelphia Pennsylvania 19104 —
Medical Univ. of South Carolina Charleston South Carolina 29425 —
Baylor Univ. Medical Center Dallas Texas 75246 —
Univ. of Wisconsin Madison Wisconsin 53792-7375 —

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00035555, 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 Jan 13, 2014 · Synced Oct 16, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00035555 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →