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Completed Phase 2 Interventional

An Open-label, Prospective, Randomized, Multi-center, Phase II Comparative Trial of Thymoglobulin Versus Simulect for the Prevention of Delayed Graft Function and Acute Allograft Rejection in Renal Allograft Recipients.

ClinicalTrials.gov ID: NCT00235300

Public ClinicalTrials.gov record NCT00235300. 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, 11:23 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

An Open-Label Prospective, Randomized, Multicenter Phase II Comparative Trial of Thymoglobulin® Versus Simulect® for the Prevention of Delayed Graft Function and Acute Allograft Rejection in Renal Allograft Recipients

Study identification

NCT ID
NCT00235300
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Genzyme, a Sanofi Company
Industry
Enrollment
240 participants

Conditions and interventions

Interventions

  • Thymoglobulin [Anti-thymocyte Globulin (rabbit)] Biological
  • Simulect (basliximab) 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
Apr 30, 2000
Primary completion
Mar 31, 2003
Completion
May 31, 2005
Last update posted
Mar 17, 2015

2000 – 2005

United States locations

U.S. sites
16
U.S. states
14
U.S. cities
16
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35296
UCLA School of Medicine Los Angeles California 90095
California Pacific Medical Center San Francisco California 94115
Yale University School of Medicine New Haven Connecticut 06510
Florida Hospital Medical Center and Translife Orlando Florida 32804
Emory University Hospital Atlanta Georgia 30322
Medical College of Georgia Augusta Georgia 30912
Rush University Transplant Program Chicago Illinois 60612
University of Kentucky Medical Center Lexington Kentucky 40536
University of Michigan Hospital Ann Arbor Michigan 48109
St. Barnabas Medical Center Livingston New Jersey 07039
Westchester Medical Center Valhalla New York 10595
Carolinas Medical Center Charlotte North Carolina 28232
Allegheny General Hospital Pittsburgh Pennsylvania 15212
University of Texas Medical Branch Galveston Texas 77555
Medical College of Wisconsin 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 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00235300, 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 17, 2015 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00235300 live on ClinicalTrials.gov.

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