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Completed Phase 2 Interventional Results available

Sorafenib/Erlotinib Versus Erlotinib Alone in Previously Treated Advanced Non-Small-Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT00600015

Public ClinicalTrials.gov record NCT00600015. 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 27, 2026, 12:47 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 Randomized Double-Blind Placebo-Controlled Phase II Trial of Sorafenib and Erlotinib or Erlotinib Alone in Previously Treated Advanced Non-Small Cell Lung Cancer

Brief summary

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

This trial will investigate the use of the newer targeted agents erlotinib and sorafenib in patients with stage IIIB or stage IV NSCLC who have received 1-2 prior chemotherapy regimens. Patients will be randomized to receive erlotinib (150 mg/day) and sorafenib (400 mg twice daily), or erlotinib (150 mg/day) and a placebo.

Study identification

NCT ID
NCT00600015
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Enrollment
166 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 31, 2008
Primary completion
Jan 31, 2009
Completion
Jan 31, 2009
Last update posted
Mar 9, 2022

2008 – 2009

United States locations

U.S. sites
16
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
Florida Cancer Specialists Fort Myers Florida 33901 —
Northeast Georgia Medical Center Gainesville Georgia 30501 —
Wellstar Cancer Research Marietta Georgia 30060 —
Kansas City Cancer Centers Overland Park Kansas 66210 —
Center for Cancer and Blood Disorders Bethesda Maryland 20817 —
Grand Rapids Clinical Oncology Program Grand Rapids Michigan 49503 —
Methodist Cancer Center Omaha Nebraska 68114 —
Cancer Care of Western North Carolina Asheville North Carolina 28801 —
Oncology Hematology Care Cincinnati Ohio 45242 —
Mid Ohio Oncology/Hematology, Inc./ The Mark H. Zangmeister Center Columbus Ohio 43219 —
South Carolina Oncology Associates, PA Columbia South Carolina 29210 —
Chattanooga Oncology Hematology Associates Chattanooga Tennessee 37404 —
Family Cancer Center Collierville Tennessee 38017 —
Tennessee Oncology, PLLC Nashville Tennessee 37023 —
Coastal Bend Cancer Center Corpus Christi Texas 78463 —
Virginia Cancer Institute Richmond Virginia 23235 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00600015, 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 Mar 9, 2022 · Synced Sep 27, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00600015 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →