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Completed Phase 2 Interventional Results available

Erlotinib (Tarceva) as a Single Agent or Intercalated With Combination Chemotherapy in Patients With EGFR Positive NSCLC

ClinicalTrials.gov ID: NCT00294762

Public ClinicalTrials.gov record NCT00294762. 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 Nov 7, 2026, 11:06 AM EST

All trial information on this site comes from the official ClinicalTrials.gov public API (clinicaltrials.gov/api/v2), run by the U.S. National Library of Medicine. We only display that public information; we do not add opinions, endorsements, or any other intent. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2 Randomized Study of Tarceva (Erlotinib) as a Single Agent or Intercalated With Combination Chemotherapy in Patients With Newly Diagnosed Advanced Non-small Cell Lung Cancer Who Have Tumors With EGFR Protein Overexpression and/or Increased EGFR Gene Copy Numbers

Brief summary

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

This will be the first prospective study where patients will be selected on the basis of two measures of the epidermal growth factor receptor (EGFR) pathway. The study will assess prospectively the efficacy of erlotinib as a single agent or intercalated with chemotherapy in highly selected patients with EGFR overexpression and/or EGFR amplification.

Study identification

NCT ID
NCT00294762
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
OSI Pharmaceuticals
Industry
Enrollment
143 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
Jan 2006 (Type not available)
Primary completion
Mar 2009 (Actual)
Completion
Mar 2009 (Actual)
Last update posted
Aug 9, 2012

2006 – 2009

United States locations

U.S. sites
38
U.S. states
20
U.S. cities
34
Facility City State ZIP Site status
Central Hematology Oncology Medical Group Inc. Alhambra California 91801 —
Comprehensive Blood and Cancer Center(Part of TORI network) Bakersfield California 93309 —
Bay Area Cancer Research Group Concord California 94520 —
Virginia K. Crosson Cancer Center Fullerton California 92835 —
Pacific Shores Medical Group Long Beach California 90813-3244 —
UCLA Medical Center Los Angeles California 90095-7077 —
North Valley Hematology/Oncology Medical GroupThe Thomas and Dorothy Leavey Cancer Center Northridge California 91325 —
Ventura County Hematology-Oncology Specialists Oxnard California 93030 —
Wilshire Oncology Medical GroupThe Robert and Beverly Lewis Family Cancer Care Center Pomona California 91767 —
Cancer Care Associates Medical Group, Inc. Redondo Beach California 90277 —
Sansum Santa Barbara Medical Foundation Clinic Santa Barbara California 93105 —
Santa Barbara Hematology Oncology Medical Group, Inc. Santa Barbara California 93105 —
University of Colorado Cancer Center Aurora Colorado 80045 —
Rocky Mountain Cancer CenterResearch Department Denver Colorado 80218 —
Eastern Connecticut Hematology and Oncology Associates Norwich Connecticut 06360-2910 —
MD Anderson Cancer Ctr - Orlando Orlando Florida 32806 —
Gulfcoast Oncology Associates Tampa Florida 33614 —
Suburban Hematology-Oncology Associates Lawrenceville Georgia 30045 —
Central Georgia Cancer Care, P.C. Macon Georgia 31201 —
Rush-Presbyterian-St.Luke's Med Ctr Chicago Illinois 60612 —
University of Chicago Medical Center Chicago Illinois 60637 —
Norton Healthcare, Inc. Louisville Kentucky 40202 —
Karmanos Cancer Institute Detroit Michigan 48201 —
Univ. of Minnesota Cancer Center Minneapolis Minnesota 55455 —
Hematology Oncology Centers of Northern Rockies Research Billings Montana 59101 —
Alegent Healthcare Omaha Nebraska 68124 —
Comprehensive Cancer Centers of Nevada Henderson Nevada 89052 —
Hematology-Oncology Associates, SJ, PA - Virtua Health Mount Holly New Jersey 08060 —
Providence Portland Medical Center Portland Oregon 97213 —
Fox Chase Cancer Center Philadelphia Pennsylvania 19111 —
Pottsville Cancer Clinic Pottsville Pennsylvania 17901 —
Boston Baskin Cancer Groupd/b/a U. of Tennessee Cancer Inst. Memphis Tennessee 38104 —
The West Cancer Clinic Memphis Tennessee 38120 —
ACORN Memphis Tennessee 38138 —
University of Texas M.D. Anderson Cancer Center Houston Texas 77030 —
Fletcher Allen Health Care Burlington Vermont 05401 —
Cancer Specialists of Tidewater, Ltd. Chesapeake Virginia 23320 —
Fred Hutchinson Cancer Research Center Seattle Washington 98109 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00294762, 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 Aug 9, 2012 · Synced Nov 7, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00294762 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →