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Completed Phase 4 Interventional Results available

Study Evaluating the Effect of Sirolimus on Non-Melanoma Skin Cancer in Kidney Transplant Recipients

ClinicalTrials.gov ID: NCT00129961

Public ClinicalTrials.gov record NCT00129961. 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 May 5, 2026, 5:29 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 Randomized, Open-Label Study to Compare the Rate of New Non-Melanoma Skin Cancer in Maintenance Renal Allograft Recipients Converted to a Sirolimus-based Regimen Versus Continuation of a Calcineurin Inhibitor-based Regimen

Study identification

NCT ID
NCT00129961
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Wyeth is now a wholly owned subsidiary of Pfizer
Industry
Enrollment
86 participants

Conditions and interventions

Interventions

  • cyclosporine or tacrolimus Drug
  • sirolimus Drug

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
Jul 31, 2005
Primary completion
Dec 31, 2008
Completion
Dec 31, 2008
Last update posted
Apr 10, 2012

2005 – 2009

United States locations

U.S. sites
12
U.S. states
11
U.S. cities
12
Facility City State ZIP Site status
Not listed San Diego California 92103
Not listed San Francisco California 94143
Not listed Gainesville Florida 32610
Not listed Atlanta Georgia 30309
Not listed Chicago Illinois 60612
Not listed Durham North Carolina 27710
Not listed Cincinnati Ohio 45267
Not listed Portland Oregon 97239
Not listed Philadelphia Pennsylvania 19102
Not listed Charleston South Carolina 29425
Not listed Nashville Tennessee 37232
Not listed Madison Wisconsin 53792

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00129961, 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 Apr 10, 2012 · Synced May 5, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00129961 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →