CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 799 enrolled / 799 target
Drug / intervention
Bevacizumab +5 morebiological
Likely dose
90 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00785291
NCT00785291Phase 3CompletedMonitor (3.8/mo)Completion was 150mo ago

A Randomized Phase III Trial of Weekly Paclitaxel Compared to Weekly Nanoparticle Albumin Bound Nab-paclitaxel or Ixabepilone With or Without Bevacizumab as First-Line Therapy for Locally Recurrent or Metastatic Breast Cancer

National Cancer Institute (NCI)·interventional·Posted Nov 5, 2008·Updated Jun 23, 2026

In Brief

A Phase 3 clinical trial evaluating Bevacizumab, Ixabepilone, and 4 other interventions for Estrogen Receptor Negative and 8 related conditions. Completed, enrolled 799 participants across 704 sites in 2 countries.

Signals

Enrolling slower than its timeline implies

Detailed Summary

This randomized phase III trial studies the side effects and how well different chemotherapy regimens with or without bevacizumab work in treating patients with stage IIIC or stage IV breast cancer. Drugs used in chemotherapy, such as paclitaxel, paclitaxel albumin-stabilized nanoparticle formulation (nab-paclitaxel), and ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. Bevacizumab may block tumor growth by targeting certain cells and slowing the growth of blood vessels to the tumor. It is not yet known which treatment regimen is more effective in treating patients with breast cancer.

Study Details

Timeline

Phase 3CompletedFinished
200920102011201220132014201520162017201820192020202120222023202420252026
First PostedNov 5, 2008
Enrollment StartOct 13, 2008
Primary CompletionDec 31, 2013
Study CompletionJun 15, 2017
TodayJul 2, 2026
Enrollment to primary: 5.2 yearsPosted 17.7 years ago

Arms & Interventions

Arm A (Paclitaxel)active_comparator

Patients receive 90 mg/m\^2 paclitaxel IV over 1 hour on days 1, 8, and 15. Patients may receive 10 mg/kg bevacizumab IV over 30-90 minutes on days 1 and 15.

Biological: BevacizumabOther: Laboratory Biomarker AnalysisDrug: PaclitaxelOther: Questionnaire Administration
Arm B (Nab-paclitaxel)experimental

Patients receive paclitaxel albumin-stabilized nanoparticle formulation IV over 30 minutes on days 1, 8, and 15. Patients may also receive 10 mg/kg bevacizumab IV over 30-90 minutes on days 1 and 15.

Biological: BevacizumabOther: Laboratory Biomarker AnalysisDrug: Nab-paclitaxelOther: Questionnaire Administration
Arm C (Ixabepilone)experimental

Patients receive ixabepilone IV over 60 minutes on days 1, 8, and 15. Patients may also receive 10 mg/kg bevacizumab IV over 30-90 minutes on days 1 and 15. (closed to accrual as of 7/18/11)

Biological: BevacizumabDrug: IxabepiloneOther: Laboratory Biomarker AnalysisOther: Questionnaire Administration

Interventions

Bevacizumabbiological

Given IV

Ixabepilonedrug

Given IV

Laboratory Biomarker Analysisother

Correlative studies

Nab-paclitaxeldrug

Given IV

Paclitaxeldrug

Given IV

Questionnaire Administrationother

Ancillary studies