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Completed Phase 2 Interventional Results available

Study of a JAK3 Inhibitor for the Prevention of Acute Rejection in Kidney Transplant Patients

ClinicalTrials.gov ID: NCT00483756

Public ClinicalTrials.gov record NCT00483756. 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 23, 2026, 11:54 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, Multicenter, Active Comparator-Controlled Trial to Evaluate the Safety and Efficacy of Co-administration of CP-690,550 and Mycophenolate Mofetil / Mycophenolate Sodium in De Novo Renal Allograft Recipients

Brief summary

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

A new immunosuppressive drug, based on the inhibition of an important enzyme in the immune system called JAK3, is being developed by Pfizer to prevent transplant rejection. In this research study, a JAK3 inhibitor or cyclosporine will be given to new kidney transplant patients for 12 months. Patients will be assigned to one of three treatment groups after receiving a kidney transplant. Two of the treatment groups will receive 2 different dosing regimens of the JAK3 inhibitor that will be taken by mouth. The third treatment group will be a standard-of-care control arm. Patients will continue to take the assigned study medication for 12 months as well as other standard transplant medications such as prednisone.

Study identification

NCT ID
NCT00483756
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
338 participants

Conditions and interventions

Interventions

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
Aug 2007 (Type not available)
Primary completion
Feb 2010 (Actual)
Completion
Apr 2010 (Actual)
Last update posted
Mar 14, 2013

2007 – 2010

United States locations

U.S. sites
37
U.S. states
18
U.S. cities
28
Facility City State ZIP Site status
Pfizer Investigational Site Little Rock Arkansas 72205 —
Pfizer Investigational Site Los Angeles California 90048 —
Pfizer Investigational Site Los Angeles California 90095 —
Pfizer Investigational Site Palo Alto California 94304 —
Pfizer Investigational Site San Diego California 92123 —
Pfizer Investigational Site San Francisco California 94115 —
Pfizer Investigational Site San Francisco California 94143 —
Pfizer Investigational Site Stanford California 94305 —
Pfizer Investigational Site Aurora Colorado 80045 —
Pfizer Investigational Site New Haven Connecticut 06504 —
Pfizer Investigational Site New Haven Connecticut 06510 —
Pfizer Investigational Site Gainesville Florida 32610 —
Pfizer Investigational Site Gainsville Florida 32610 —
Pfizer Investigational Site Tampa Florida 33606 —
Pfizer Investigational Site Chicago Illinois 60611 —
Pfizer Investigational Site Chicago Illinois 60637 —
Pfizer Investigational Site Baltimore Maryland 21201 —
Pfizer Investigational Site Boston Massachusetts 02215 —
Pfizer Investigational Site Springfield Massachusetts 01107 —
Pfizer Investigational Site Springfield Massachusetts 01199 —
Pfizer Investigational Site Ann Arbor Michigan 48109 —
Pfizer Investigational Site Detroit Michigan 48202 —
Pfizer Investigational Site Rochester Minnesota 55905 —
Pfizer Investigational Site St Louis Missouri 63110 —
Pfizer Investigational Site Livingston New Jersey 07039 —
Pfizer Investigational Site New York New York 10029 —
Pfizer Investigational Site Valhalla New York 10595 —
Pfizer Investigational Site Chapel Hill North Carolina 27514 —
Pfizer Investigational Site Chapel Hill North Carolina 27599-7155 —
Pfizer Investigational Site Chapel Hill North Carolina 27599-7211 —
Pfizer Investigational Site Chapel Hill North Carolina 27599-7360 —
Pfizer Investigational Site Portland Oregon 97239 —
Pfizer Investigational Site Philadelphia Pennsylvania 19102 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site Dallas Texas 75204 —
Pfizer Investigational Site Dallas Texas 75246 —
Pfizer Investigational Site Fort Worth Texas 76104 —

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 32 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00483756, 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 14, 2013 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00483756 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →