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NCT00390156 · ClinicalTrials.gov registry record · Phase 1

Imatinib, Bevacizumab, and Cyclophosphamide in Patients With Refractory Metastatic Solid Tumors

A Phase 1 study, sponsored by University of California, San Francisco.

Completed
Registry status
Phase 1
Development phase
35
Enrollment target

NCT00390156 is a Phase 1 study that has completed, run by University of California, San Francisco. The registered enrollment target is 35 participants.

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The verdict

NCT00390156, a Phase 1 study, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
Phase 1
Development phase
35 participants
Enrollment target

Study Summary

RATIONALE: Imatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. 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. Drugs used in chemotherapy, such as cyclophosphamide, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Bevacizumab and cyclophosphamide may also stop the growth of tumor cells by blocking blood flow to the tumor. Imatinib and bevacizumab may help cyclophosphamide work better by making tumor cells more sensitive to the drug. Giving cyclophosphamide once a day together with imatinib and bevacizumab may kill more tumor cells. PURPOSE: This phase I trial is studying the side effects and best dose of imatinib when given together with bevacizumab and cyclophosphamide in treating patients with refractory metastatic solid tumors.

Interventions

  • DRUG cyclophosphamide
  • DRUG imatinib
  • BIOLOGICAL bevacizumab

Trial Details

FieldValue
Enrollment Target 35 participants
Start Date 2006-08
Est. Completion 2011-01
Phase Phase 1

What the Registry Record Tells You About NCT00390156

The ClinicalTrials.gov registry entry for NCT00390156 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 35 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 3 interventions - of which cyclophosphamide is the first listed.

NCT00390156 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00390156 about?

NCT00390156 is a clinical study titled "Imatinib, Bevacizumab, and Cyclophosphamide in Patients With Refractory Metastatic Solid Tumors". RATIONALE: Imatinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. 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...

What is the current status of trial NCT00390156?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 35 participants. The study started on 2006-08. Estimated completion is 2011-01.

What interventions are being tested in trial NCT00390156?

The interventions under investigation include: cyclophosphamide (DRUG), imatinib (DRUG), bevacizumab (BIOLOGICAL).

Who is sponsoring clinical trial NCT00390156?

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.