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Completed Phase 2 Interventional

Trial of Carboplatin/Paclitaxel/Cetuximab in Stage IIIB/IV Non-Small Cell Lung Cancer (NSCLC)

ClinicalTrials.gov ID: NCT00097227

Public ClinicalTrials.gov record NCT00097227. 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 4, 2026, 9:59 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

A Randomized Phase II Trial of Two Dose Schedules of Carboplatin/Paclitaxel/Cetuximab in Stage IIIB/IV Non-small Cell Lung Cancer

Brief summary

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

The purpose of the study is to determine if the combination of cetuximab, carboplatin and paclitaxel will shrink a specific type of lung cancer known as non-small cell lung cancer (NSCLC). The safety of this combination will also be evaluated.

Study identification

NCT ID
NCT00097227
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Eli Lilly and Company
Industry
Enrollment
165 participants

Conditions and interventions

Interventions

Biological · 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
Oct 31, 2004
Primary completion
Mar 31, 2007
Completion
Mar 31, 2007
Last update posted
Apr 8, 2010

2004 – 2007

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
ImClone Investigational Site Los Angeles California 90089
ImClone Investigational Site Santa Monica California 90404
ImClone Investigational Site Newark Delaware 19713
ImClone Investigational Site Orlando Florida 32804
ImClone Investigational Site St. Petersburg Florida 33705
ImClone Investigational Site Tucker Georgia 30084
ImClone Investigational Site Terra Haute Indiana 47804
ImClone Investigational Site Louisville Kentucky 40202
ImClone Investigational Site Baltimore Maryland 21204
ImClone Investigational Site Ypsilanti Michigan 48197
ImClone Investigational Site Newark New Jersey 07112
ImClone Investigational Site Chapel Hill North Carolina 27599
ImClone Investigational Site Philadelphia Pennsylvania 19141
ImClone Investigational Site Columbia South Carolina 29209
ImClone Investigational Site Knoxville Tennessee 37920
ImClone Investigational Site Houston Texas 77024
ImClone Investigational Site Temple Texas 76508
ImClone Investigational Site Richmond Virginia 23230
ImClone Investigational Site Tacoma Washington 98405
ImClone Investigational Site Morgantown West Virginia 26506

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 NCT00097227, 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 Apr 8, 2010 · Synced Sep 4, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00097227 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →