Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00483756 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study of Kidney Transplantation, sponsored by Pfizer.

Completed
Registry status
Phase 2
Development phase
338
Enrollment target
20
Study locations

NCT00483756: Completed Phase 2 study of Kidney Transplantation, sponsored by Pfizer.

NCT00483756 is a Phase 2 study of Kidney Transplantation that has completed, run by Pfizer. The registered enrollment target is 338 participants, above the 258-participant average among 33 other Kidney Transplantation trials with a reported enrollment target (31% higher). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00483756, a Phase 2 study of Kidney Transplantation, has completed, sponsored by Pfizer.

COMPLETED
Registry status
Phase 2
Development phase
338 participants
Enrollment target
20
Study locations

Study Summary

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.

Primary Outcome

Clinical BPAR was a BPAR (category acute rejection as interpreted by the central blinded pathologist according to the Banff 97 working classification) associated with an increase in serum creatinine of \>= 0.3 milligram per deciliter (mg/dL) and \>=20 percent (%) from pre-rejection baseline. The increase in serum creatinine was assessed based on the comparison of baseline and the highest serum creatinine recorded within 24 hours (hrs) of the time of biopsy.

Conditions Studied

Interventions

  • DRUG Cyclosporine
  • DRUG CP-690,550

Study Locations (20)

California

  • Pfizer Investigational Site - Los Angeles
  • Pfizer Investigational Site - Los Angeles
  • Pfizer Investigational Site - Palo Alto
  • Pfizer Investigational Site - San Diego
  • Pfizer Investigational Site - San Francisco
  • Pfizer Investigational Site - San Francisco
  • Pfizer Investigational Site - Stanford

Florida

  • Pfizer Investigational Site - Gainesville
  • Pfizer Investigational Site - Gainsville
  • Pfizer Investigational Site - Tampa

Massachusetts

  • Pfizer Investigational Site - Boston
  • Pfizer Investigational Site - Springfield
  • Pfizer Investigational Site - Springfield

Connecticut

  • Pfizer Investigational Site - New Haven
  • Pfizer Investigational Site - New Haven

Illinois

  • Pfizer Investigational Site - Chicago
  • Pfizer Investigational Site - Chicago

Arkansas

  • Pfizer Investigational Site - Little Rock

Colorado

  • Pfizer Investigational Site - Aurora

Maryland

  • Pfizer Investigational Site - Baltimore

Trial Details

FieldValue
Enrollment Target 338 participants
Start Date 2007-08
Est. Completion 2010-04
Phase Phase 2
Pfizer

1,845 total trials

What the finished NCT00483756 record still lists

NCT00483756 is an interventional study that assigns participants to a tested intervention. The registered 338 participants enrollment target is mid-sized for trials with a published cap, above the 258-participant average among 33 other Kidney Transplantation trials with a reported enrollment target (31% higher).

The record links to 1 condition, with Kidney Transplantation appearing as the primary indexed condition, and to 2 interventions - of which Cyclosporine is the first listed.

NCT00483756 names 20 study sites across 8 states, led by California, Florida, Massachusetts.

Frequently Asked Questions

What is clinical trial NCT00483756 about?

NCT00483756 is a clinical study titled "Study of a JAK3 Inhibitor for the Prevention of Acute Rejection in Kidney Transplant Patients". 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. Patient...

What is the current status of trial NCT00483756?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 338 participants. The study started on 2007-08. Estimated completion is 2010-04.

What conditions does trial NCT00483756 study?

This clinical trial studies the following conditions: Kidney Transplantation.

What interventions are being tested in trial NCT00483756?

The interventions under investigation include: Cyclosporine (DRUG), CP-690,550 (DRUG).

Who is sponsoring clinical trial NCT00483756?

This trial is sponsored by Pfizer, which has 1,845 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00483756 being conducted?

This trial has 20 study locations across Arkansas, California, Colorado, Connecticut, Florida. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Kidney Transplantation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT00483756's enrollment target sits among peer trials

338 7th of 33 higher than 27 of 33 other Kidney Transplantation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Kidney Transplantation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT03253263 · 338 participants · Phase 2

    A Clinical Efficacy and Safety Study of OHB-607 in Preventing Bronchopulmonary Dysplasia in Extremely Premature Infants

  • NCT05658731 · 338 participants · NA

    Cognitive Outcomes After Brain Substructure-informed Radiation Planning in Pediatric Patients

  • NCT06022939 · 338 participants · Phase 3

    Comparing Dara-VCD Chemotherapy Plus Stem Cell Transplant to Dara-VCD Chemotherapy Alone for People Who Have Newly Diagnosed AL Amyloidosis

  • NCT04176172 · 340 participants · Phase 3

    Optimizing Tobacco Use Treatment for PLWHA

Similar registry start date

  • NCT05988463 · started 2027-01-01 · Phase 1

    Dose-Escalation Study of Artesunate Patients With IPF

  • NCT07219706 · started 2026-12-10 · NA

    Dietary Fiber and Time Restricted Eating

  • NCT02831335 · started 2026-12-01

    Technical Development of Multi-Parametric Renocerebral MRI

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

Source: ClinicalTrials.gov NCT00483756, the US trial registry maintained by the National Library of Medicine. NCT00483756 (mid enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.