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Transplant Surgery »  Research »  Clinical Trials »  A3921050 LTE

Extension Study Of Subjects From Study A3921030 For The Prevention Of Acute Rejection In Kidney Transplant Patients

Official Title:

A Phase 2, Multicenter, Open-Label, Active Comparator-Controlled, Extension Trial To Evaluate The Long-Term Safety And Efficacy Of CP-690,550 In Renal Allograft Recipients

Basic Trial Information

Phase Type Age Sponsor Protocol IDs Status
Phase 2 Interventional 18 - 70 Years Pfizer A3921050
NCT00658359
Active, but closed to enrollment

Study Design:

Prevention, Open Label, Parallel Assignment, Safety/Efficacy Study

Principal Investigator

Flavio Vincenti, M.D.

Professor of Clinical Medicine
Division of Nephrology
Departments of Medicine and Surgery

 

Trial Summary

This is a study that will follow transplant patients from Study A3921030 to monitor for long term safety, tolerability and efficacy for 2 additional years. Patients will continue their study medications that were previously assigned.

Eligibility

Inclusion Criteria:
  • Subjects who successfully completed Study A3921030
Exclusion Criteria:
  • Subjects who are on the waiting list for a second kidney transplant or any non-renal
    organ transplants

Important

Final eligibility is determined by the health professionals conducting the trial and the protocol approved by the Committee on Human Resources (CHR) at the University of California, San Francisco (UCSF). The Patient Consent Form for this trial is available upon request. For more information about this trial, please see the full posting at ClinicalTrials.gov.

For More Information

For questions about this trial or eligibility, contact:

Clarina Mendoza
(415) 353-8380
Clarina.Mendoza@ucsfmedctr.org

Information about this trial was obtained from the NIH Clinical Trials website, http://clinicaltrials.gov on 10/22/2009. UCSF specific information including the PI (Principal Investigator), trial enrollment status, and UCSF Study ID, supplement the ClinicalTrials.gov study posting.
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