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NCT00293332 · ClinicalTrials.gov registry record · Phase 2

Docetaxel, Carboplatin, and Bevacizumab in Treating Patients With Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer That Can Be Removed By Surgery

A Phase 2 study, sponsored by University of California, San Francisco.

Terminated
Registry status
Phase 2
Development phase
1
Enrollment target

NCT00293332 is a Phase 2 study that was terminated before completion, run by University of California, San Francisco. The registered enrollment target is 1 participants.

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The verdict

NCT00293332, a Phase 2 study, was terminated before completion, sponsored by University of California, San Francisco.

TERMINATED
Registry status
Phase 2
Development phase
1 participants
Enrollment target

Study Summary

RATIONALE: Drugs used in chemotherapy, such as docetaxel and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, 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. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Giving docetaxel and carboplatin together with bevacizumab before surgery may make the tumor smaller and reduce the amount of normal tissue that needs to be removed. PURPOSE: This phase II trial is studying how well giving docetaxel and carboplatin together with bevacizumab works in treating patients with stage I, stage II, or stage III non-small cell lung cancer that can be removed by surgery.

Interventions

  • DRUG carboplatin
  • DRUG docetaxel
  • PROCEDURE conventional surgery
  • BIOLOGICAL bevacizumab

Trial Details

FieldValue
Enrollment Target 1 participants
Start Date 2005-12
Est. Completion 2007-04
Phase Phase 2

What the Registry Record Tells You About NCT00293332

The ClinicalTrials.gov registry entry for NCT00293332 describes a study currently listed as terminated, categorized as Phase 2. The registered enrollment target is 1 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 4 interventions - of which carboplatin is the first listed.

NCT00293332 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00293332 about?

NCT00293332 is a clinical study titled "Docetaxel, Carboplatin, and Bevacizumab in Treating Patients With Stage I, Stage II, or Stage III Non-Small Cell Lung Cancer That Can Be Removed By Surgery". RATIONALE: Drugs used in chemotherapy, such as docetaxel and carboplatin, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some block the abil...

What is the current status of trial NCT00293332?

This trial is currently terminated. It is a Phase 2 study. The enrollment target is 1 participants. The study started on 2005-12. Estimated completion is 2007-04.

What interventions are being tested in trial NCT00293332?

The interventions under investigation include: carboplatin (DRUG), docetaxel (DRUG), conventional surgery (PROCEDURE), bevacizumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00293332?

This trial is sponsored by University of California, San Francisco, which has 1,713 total clinical trials registered on ClinicalTrials.gov.

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

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.