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Completed Phase 1 Interventional

Cetuximab, Cisplatin, and Radiation Therapy in Treating Patients With Stage IB, Stage II, Stage III, or Stage IVA Cervical Cancer

ClinicalTrials.gov ID: NCT00104910

Public ClinicalTrials.gov record NCT00104910. 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 11, 2026, 1:40 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 I Trial of Tailored Radiation Therapy With Concomitant Cetuximab (C225, NSC #714692) and Cisplatin (NSC #119875) in the Treatment of Patients With Cervical Cancer

Brief summary

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

This phase I trial is studying the side effects and best dose of cetuximab when given together with cisplatin and radiation therapy in treating patients with stage IB, stage II, stage III, or stage IVA cervical cancer. Monoclonal antibodies, such as cetuximab, can block tumor growth in different ways. Some block the ability of tumor cells to grow and spread. Others find tumor cells and help kill them or carry tumor-killing substances to them. Drugs used in chemotherapy, such as cisplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Radiation therapy uses high-energy x-rays and other types of radiation to kill tumor cells. Internal radiation therapy uses radioactive material placed directly into or near a tumor to kill tumor cells. Giving cetuximab together with cisplatin and radiation therapy may kill more tumor cells.

Study identification

NCT ID
NCT00104910
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
64 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
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
Dec 31, 2004
Primary completion
Dec 31, 2012
Completion
Not listed
Last update posted
Dec 30, 2014

Started 2005

United States locations

U.S. sites
15
U.S. states
10
U.S. cities
13
Facility City State ZIP Site status
Georgia Regents University Medical Center Augusta Georgia 30912
University of Chicago Comprehensive Cancer Center Chicago Illinois 60637
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202
University of Iowa Hospitals and Clinics Iowa City Iowa 52242
Johns Hopkins University/Sidney Kimmel Comprehensive Cancer Center Baltimore Maryland 21287
Cooper Hospital University Medical Center Camden New Jersey 08103
MetroHealth Medical Center Cleveland Ohio 44109
Cleveland Clinic Foundation Cleveland Ohio 44195
Riverside Methodist Hospital Columbus Ohio 43214
Lake University Ireland Cancer Center Mentor Ohio 44060
University of Oklahoma Health Sciences Center Oklahoma City Oklahoma 73104
Women and Infants Hospital Providence Rhode Island 02905
Parkland Memorial Hospital Dallas Texas 75235
University of Texas Southwestern Medical Center Dallas Texas 75390
M D Anderson Cancer Center Houston Texas 77030

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 NCT00104910, 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 Dec 30, 2014 · Synced Sep 11, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00104910 live on ClinicalTrials.gov.

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