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Completed Phase 4 Interventional Results available

A Study to Evaluate the Efficacy and Safety of Zenapax in Combination With CellCept, Cyclosporine, and Corticosteroids in Patients Undergoing Cardiac Transplantation

ClinicalTrials.gov ID: NCT00048165

Public ClinicalTrials.gov record NCT00048165. 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 Sep 2, 2026, 3:51 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

A Double-Blind, Placebo -Controlled, Randomized Study to Assess the Efficacy and Safety of Zenapax in Combination With CellCept, Cyclosporine, and Corticosteroids in Patients Undergoing Cardiac Transplantation.

Brief summary

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

The purpose of the study is to compare the number of randomized participants in each treatment group who experience an acute rejection episode in the first 6 months after undergoing cardiac transplantation.

Study identification

NCT ID
NCT00048165
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
434 participants

Conditions and interventions

Eligibility (public fields only)

Age range
13 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
Jul 31, 1999
Primary completion
Jul 31, 2002
Completion
Jul 31, 2002
Last update posted
Jun 12, 2016

1999 – 2002

United States locations

U.S. sites
25
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294-0006
Not listed Los Angeles California 90095
Not listed Tampa Florida 33606
Not listed Louisville Kentucky 40202
Not listed Baltimore Maryland 21287
Not listed Boston Massachusetts 02111
Not listed Boston Massachusetts 02115
Not listed Ann Arbor Michigan 48109-0366
Not listed Minneapolis Minnesota 55455
Not listed Albuquerque New Mexico 87106
Not listed New York New York 10032
Not listed Durham North Carolina 27710
Not listed Cincinnati Ohio 45267-0542
Not listed Cleveland Ohio 44195
Not listed Portland Oregon 97201
Not listed Philadelphia Pennsylvania 19104
Not listed Philadelphia Pennsylvania 19140
Not listed Pittsburgh Pennsylvania 15213-2582
Not listed Charleston South Carolina 29425-2221
Not listed Dallas Texas 75230
Not listed Dallas Texas 75246
Not listed Houston Texas 77030
Not listed Salt Lake City Utah 84132
Not listed Madison Wisconsin 53792
Not listed Milwaukee Wisconsin 53215

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00048165, 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 Jun 12, 2016 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00048165 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →