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NCT00101192 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Gynecologic Oncology Group.

Completed
Registry status
Phase 2
Development phase
76
Enrollment target

NCT00101192 is a Phase 2 study that has completed, run by Gynecologic Oncology Group. The registered enrollment target is 76 participants.

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The verdict

NCT00101192, a Phase 2 study, has completed, sponsored by Gynecologic Oncology Group.

COMPLETED
Registry status
Phase 2
Development phase
76 participants
Enrollment target

Study Summary

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.

Interventions

  • DRUG cisplatin
  • BIOLOGICAL cetuximab

Trial Details

FieldValue
Enrollment Target 76 participants
Start Date 2004-09
Phase Phase 2

Sponsor

Gynecologic Oncology Group

154 total trials

What the Registry Record Tells You About NCT00101192

The ClinicalTrials.gov registry entry for NCT00101192 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 76 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Gynecologic Oncology Group, which has 154 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which cisplatin is the first listed.

NCT00101192 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00101192 about?

NCT00101192 is a clinical study titled "Cetuximab and Cisplatin in Treating Patients With Advanced, Persistent, or Recurrent Cervical Cancer". 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...

What is the current status of trial NCT00101192?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 76 participants. The study started on 2004-09.

What interventions are being tested in trial NCT00101192?

The interventions under investigation include: cisplatin (DRUG), cetuximab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00101192?

This trial is sponsored by Gynecologic Oncology Group, which has 154 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.