ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

Study Evaluating A Planned Transition From Tacrolimus To Sirolimus In Kidney Transplant Recipients

ClinicalTrials.gov ID: NCT00895583

Public ClinicalTrials.gov record NCT00895583. 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 20, 2026, 11:44 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

Planned Transition To Sirolimus-Based Therapy Versus Continued Tacrolimus-Based Therapy In Renal Allograft Recipients

Study identification

NCT ID
NCT00895583
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Pfizer
Industry
Enrollment
254 participants

Conditions and interventions

Interventions

  • Sirolimus Drug
  • Tacrolimus 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
May 31, 2009
Primary completion
Jul 31, 2013
Completion
Jul 31, 2013
Last update posted
Sep 17, 2014

2009 – 2013

United States locations

U.S. sites
25
U.S. states
16
U.S. cities
22
Facility City State ZIP Site status
Pfizer Investigational Site La Jolla California 92037
Pfizer Investigational Site San Francisco California 94115
Pfizer Investigational Site Aurora Colorado 80045
Pfizer Investigational Site Denver Colorado 80230
Pfizer Investigational Site Atlanta Georgia 30309
Pfizer Investigational Site Chicago Illinois 60611
Pfizer Investigational Site Lexington Kentucky 40536
Pfizer Investigational Site Portland Maine 04102
Pfizer Investigational Site Boston Massachusetts 02215
Pfizer Investigational Site Detroit Michigan 48202
Pfizer Investigational Site Detroit Michigan 48236
Pfizer Investigational Site New York New York 10032
Pfizer Investigational Site Rochester New York 14642
Pfizer Investigational Site Chapel Hill North Carolina 27599 7155
Pfizer Investigational Site Durham North Carolina 27705
Pfizer Investigational Site Cincinnati Ohio 45267-0589
Pfizer Investigational Site Cincinnati Ohio 45267-0595
Pfizer Investigational Site Cleveland Ohio 44106
Pfizer Investigational Site Portland Oregon 97239
Pfizer Investigational Site Philadelphia Pennsylvania 19107
Pfizer Investigational Site Charleston South Carolina 29425
Pfizer Investigational Site Houston Texas 77030
Pfizer Investigational Site Charlottesville Virginia 22901
Pfizer Investigational Site Charlottesville Virginia 22908
Pfizer Investigational Site Richmond Virginia 23298

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 19 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00895583, 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 Sep 17, 2014 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00895583 live on ClinicalTrials.gov.

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