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Terminated Phase 2 Interventional

A Study to Evaluate the Safety and Efficacy of Prograf/FK778 and Prograf/MMF in de Novo Kidney Transplant Recipients

ClinicalTrials.gov ID: NCT00282230

Public ClinicalTrials.gov record NCT00282230. 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 24, 2026, 12:55 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 Phase 2, Randomized, Open-Label, Parallel Group, Multi-Center Study to Assess the Safety and Efficacy of Prograf®/FK778 and Prograf®/MMF in De Novo Kidney Transplant Recipients

Brief summary

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

A study to evaluate the safety and efficacy of Prograf/FK778 in de novo kidney transplant patients

Study identification

NCT ID
NCT00282230
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Astellas Pharma Inc
Industry
Enrollment
150 participants

Conditions and interventions

Interventions

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
Nov 2003 (Type not available)
Primary completion
Not listed
Completion
Oct 2005 (Actual)
Last update posted
Jun 7, 2012

2003 – 2005

United States locations

U.S. sites
23
U.S. states
18
U.S. cities
22
Facility City State ZIP Site status
Not listed Birmingham Alabama 35294 —
Not listed Los Angeles California 90057 —
Not listed San Diego California 92123 —
Not listed Denver Colorado 80262 —
Not listed Washington D.C. District of Columbia 20010 —
Not listed Jacksonville Florida 32216 —
Not listed Miami Florida 33136 —
Not listed Chicago Illinois 60637 —
Not listed Indianapolis Indiana 46202 —
Not listed Wichita Kansas 67214 —
Not listed New Orleans Louisiana 70121 —
Not listed Detroit Michigan 80262 —
Not listed New Brunswick New Jersey 89003 —
Not listed New York New York 10021 —
Not listed New York New York 10029 —
Not listed Durham North Carolina 27710 —
Not listed Cincinnati Ohio 45267 —
Not listed Harrisburg Pennsylvania 17104 —
Not listed Philadelphia Pennsylvania 19107 —
Not listed Memphis Tennessee 38163 —
Not listed Salt Lake City Utah 84132 —
Not listed Madison Wisconsin 53792 —
Not listed 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.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00282230, 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 7, 2012 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00282230 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →