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NCT00305825 · ClinicalTrials.gov registry record · Phase 2

Bevacizumab and Letrozole in Treating Postmenopausal Women With Locally Advanced or Metastatic Breast Cancer That Cannot Be Removed By Surgery

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

Completed
Registry status
Phase 2
Development phase
43
Enrollment target
2
Study locations

NCT00305825 is a Phase 2 study of Breast Cancer that has completed, run by University of California, San Francisco. The registered enrollment target is 43 participants, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The trial reports 2 study locations across 2 states.

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The verdict

NCT00305825, a Phase 2 study of Breast Cancer, has completed, sponsored by University of California, San Francisco.

COMPLETED
Registry status
Phase 2
Development phase
43 participants
Enrollment target
2
Study locations

Study Summary

RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some find tumor cells and kill them or carry tumor-killing substances to them. Others interfere with the ability of tumor cells to grow and spread. Bevacizumab may also stop the growth of tumor cells by blocking blood flow to the tumor. Estrogen can cause the growth of breast cancer cells. Hormone therapy using letrozole may fight breast cancer by lowering the amount of estrogen the body makes. Giving bevacizumab together with letrozole may be an effective treatment for locally advanced or metastatic breast cancer. PURPOSE: This phase II trial is studying how well giving bevacizumab together with letrozole works in treating postmenopausal women with locally advanced or metastatic breast cancer that cannot be removed by surgery.

Conditions Studied

Interventions

  • DRUG letrozole
  • BIOLOGICAL bevacizumab

Study Locations (2)

California

  • UCSF Comprehensive Cancer Center - San Francisco

New York

  • Memorial Sloan-Kettering Cancer Center - New York

Trial Details

FieldValue
Enrollment Target 43 participants
Start Date 2004-08
Est. Completion 2016-05-24
Phase Phase 2

What the Registry Record Tells You About NCT00305825

The ClinicalTrials.gov registry entry for NCT00305825 describes a study currently listed as completed, categorized as Phase 2. The registered enrollment target is 43 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,803-participant average among 1,224 other Breast Cancer trials with a reported enrollment target (98% lower). The listed sponsor is University of California, San Francisco, which has 1,713 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Breast Cancer appearing as the primary indexed condition, and to 2 interventions - of which letrozole is the first listed.

NCT00305825 reports 2 study locations spanning 2 distinct geographic areas - top geographies include California, New York.

Frequently Asked Questions

What is clinical trial NCT00305825 about?

NCT00305825 is a clinical study titled "Bevacizumab and Letrozole in Treating Postmenopausal Women With Locally Advanced or Metastatic Breast Cancer That Cannot Be Removed By Surgery". RATIONALE: Monoclonal antibodies, such as bevacizumab, can block tumor growth in different ways. Some find tumor cells and kill them or carry tumor-killing substances to them. Others interfere with the ability of tumor cells to grow and spread. Bevacizumab may also stop the growth of tumor cells by ...

What is the current status of trial NCT00305825?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 43 participants. The study started on 2004-08. Estimated completion is 2016-05-24.

What conditions does trial NCT00305825 study?

This clinical trial studies the following conditions: Breast Cancer.

What interventions are being tested in trial NCT00305825?

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

Who is sponsoring clinical trial NCT00305825?

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

Where is trial NCT00305825 being conducted?

This trial has 2 study locations across California, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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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.