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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 Oct 25, 2026, 7:41 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
Jul 2003 (Type not available)
Primary completion
Jun 2006 (Actual)
Completion
Mar 2011 (Actual)
Last update posted
Oct 25, 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 25, 2012 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00065468 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →