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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 Jul 21, 2026, 6:44 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

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

  • cetuximab Biological
  • cisplatin Drug

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
Aug 31, 2004
Primary completion
Jun 30, 2011
Completion
Not listed
Last update posted
Mar 16, 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 16, 2014 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00101192 live on ClinicalTrials.gov.

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