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Completed Phase 2 Interventional Results available

Cetuximab and Cisplatin in Treating Patients With Advanced, Persistent, or Recurrent Cervical Cancer

ClinicalTrials.gov ID: NCT00101192

Public ClinicalTrials.gov record NCT00101192. 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 28, 2026, 12:24 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 Limited Access Phase II Trial of Cetuximab (C225, NSC #714692) in Combination With Cisplatin (NSC #119875) in the Treatment of Advanced, Persistent, or Recurrent Carcinoma of the Cervix

Brief summary

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

RATIONALE: 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. Cetuximab may also help cisplatin work better by making tumor cells more sensitive to the drug. 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. Giving cetuximab together with cisplatin may be a better way to block tumor growth. PURPOSE: This phase II trial is studying how well giving cetuximab together with cisplatin works in treating patients with advanced, persistent, or recurrent cervical cancer.

Study identification

NCT ID
NCT00101192
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Gynecologic Oncology Group
Network
Enrollment
76 participants

Conditions and interventions

Interventions

Biological · Drug

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
Sep 2004 (Type not available)
Primary completion
Jul 2011 (Actual)
Completion
Not listed
Last update posted
Mar 17, 2014

Started 2004

United States locations

U.S. sites
18
U.S. states
12
U.S. cities
17
Facility City State ZIP Site status
Providence Saint Joseph Medical Center - Burbank Burbank California 91505 —
USC/Norris Comprehensive Cancer Center and Hospital Los Angeles California 90089-9181 —
Curtis and Elizabeth Anderson Cancer Institute at Memorial Health University Medical Center Savannah Georgia 31403-3089 —
Indiana University Melvin and Bren Simon Cancer Center Indianapolis Indiana 46202-5289 —
Kansas Masonic Cancer Research Institute at the University of Kansas Medical Center Kansas City Kansas 66160-7357 —
Ochsner Cancer Institute at Ochsner Clinic Foundation New Orleans Louisiana 70121 —
Christus Schumpert Cancer Treatment Center Shreveport Louisiana 71101 —
University of Mississippi Cancer Clinic Jackson Mississippi 39216 —
Fox Chase Virtua Health Cancer Program at Virtua West Jersey Voorhees Township New Jersey 08043 —
Wake Forest University Comprehensive Cancer Center Winston-Salem North Carolina 27157-1096 —
MetroHealth Cancer Care Center at MetroHealth Medical Center Cleveland Ohio 44109 —
Cleveland Clinic Taussig Cancer Center Cleveland Ohio 44195 —
Oklahoma University Cancer Institute Oklahoma City Oklahoma 73104 —
Cancer Care Associates - Midtown Tulsa Tulsa Oklahoma 74104 —
Fox Chase Cancer Center - Philadelphia Philadelphia Pennsylvania 19111-2497 —
McGlinn Family Regional Cancer Center at Reading Hospital and Medical Center Reading Pennsylvania 19612-6052 —
University of Texas Medical Branch Galveston Texas 77555-0361 —
M. D. Anderson Cancer Center at University of Texas Houston Texas 77030-4009 —

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 NCT00101192, 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 17, 2014 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00101192 live on ClinicalTrials.gov.

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