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Completed Phase 3 Interventional Results available

Study Evaluating Interferon And CCI-779 In Advanced Renal Cell Carcinoma

ClinicalTrials.gov ID: NCT00065468

Public ClinicalTrials.gov record NCT00065468. 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 Sep 5, 2026, 5:27 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 3, Three-Arm, Randomized, Open-Label Study Of Interferon Alfa Alone, CCI-779 Alone, And The Combination Of Interferon Alfa And CCI-779 In First-Line Poor-Prognosis Subjects With Advanced Renal Cell Carcinoma.

Brief summary

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

The primary objective of this study is efficacy. The primary efficacy endpoint of this study is a comparison of the overall survival of subjects treated with CCI-779 \[Temsirolimus\], administered intravenously \[IV\] once weekly and the combination of CCI-779, administered IV once weekly with Interferon Alfa \[IFN alfa\] subcutaneously \[SC\] three times per week \[TIW\], compared with the overall survival of subjects treated with IFN alfa (SC TIW) alone, in poor-prognosis subjects with advanced RCC.

Study identification

NCT ID
NCT00065468
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
626 participants

Conditions and interventions

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
Jun 30, 2003
Primary completion
May 31, 2006
Completion
Feb 28, 2011
Last update posted
Oct 24, 2012

2003 – 2011

United States locations

U.S. sites
48
U.S. states
28
U.S. cities
47
Facility City State ZIP Site status
Pfizer Investigational Site Little Rock Arkansas 72205
Pfizer Investigational Site La Verne California 91750
Pfizer Investigational Site Los Angeles California 90024-2828
Pfizer Investigational Site San Diego California 92123
Pfizer Investigational Site San Francisco California 94115
Pfizer Investigational Site Waterbury Connecticut 06708
Pfizer Investigational Site Boca Raton Florida 33428
Pfizer Investigational Site Miami Florida 33136
Pfizer Investigational Site Chicago Illinois 60612-3824
Pfizer Investigational Site Urbana Illinois 61801
Pfizer Investigational Site Indianapolis Indiana 46303
Pfizer Investigational Site South Bend Indiana 46601
Pfizer Investigational Site Terre Haute Indiana 47802
Pfizer Investigational Site Kansas City Kansas 66160-7136
Pfizer Investigational Site Louisville Kentucky 40202
Pfizer Investigational Site New Orleans Louisiana 70121
Pfizer Investigational Site Baltimore Maryland 21231-1000
Pfizer Investigational Site Boston Massachusetts 02215
Pfizer Investigational Site Ann Arbor Michigan 48109-0942
Pfizer Investigational Site Detroit Michigan 48202
Pfizer Investigational Site Kansas City Missouri 64131
Pfizer Investigational Site St Louis Missouri 63110
Pfizer Investigational Site Billings Montana 59101
Pfizer Investigational Site Great Falls Montana 59405
Pfizer Investigational Site Lebanon New Hampshire 03766
Pfizer Investigational Site East Orange New Jersey 07018
Pfizer Investigational Site Morristown New Jersey 07960
Pfizer Investigational Site New York New York 10021
Pfizer Investigational Site Rochester New York 14642
Pfizer Investigational Site The Bronx New York 10466
Pfizer Investigational Site Valhalla New York 10595
Pfizer Investigational Site Durham North Carolina 27710
Pfizer Investigational Site Hickory North Carolina 28602
Pfizer Investigational Site Cleveland Ohio 44195
Pfizer Investigational Site Oklahoma City Oklahoma 73104
Pfizer Investigational Site Portland Oregon 97213-2933
Pfizer Investigational Site Hershey Pennsylvania 17033-0850
Pfizer Investigational Site Philadelphia Pennsylvania 19111
Pfizer Investigational Site Pittsburgh Pennsylvania 15213
Pfizer Investigational Site Charleston South Carolina 29414
Pfizer Investigational Site Knoxville Tennessee 37920
Pfizer Investigational Site Memphis Tennessee 38120
Pfizer Investigational Site Nashville Tennessee 37232-6310
Pfizer Investigational Site Houston Texas 77030
Pfizer Investigational Site Salt Lake City Utah 84112
Pfizer Investigational Site Richmond Virginia 23249
Pfizer Investigational Site Seattle Washington 98101
Pfizer Investigational Site Seattle Washington 98109-1023

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 105 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00065468, 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 Oct 24, 2012 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00065468 live on ClinicalTrials.gov.

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