CI

At a glance

ClinicalIndex Comparison Record
Phase 3Completed· 564 enrolled
Drug / intervention
Bevacizumab and Paclitaxel +1 morebiological
Likely dose
Bevacizumab and Paclitaxel 10 mg/kgfrom 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.

In the news

1 article

Matched to this trial by ClinicalIndexfrom reputable biotech & medical press.

Search/NCT00600340
NCT00600340Phase 3Completed

A Randomized Phase III 2-arm Trial of Paclitaxel Plus Bevacizumab vs. Capecitabine Plus Bevacizumab for the First-line Treatment of Human Epidermal Growth Factor Receptor 2 (HER2)-Negative Locally Recurrent or Metastatic Breast Cancer

Central European Cooperative Oncology Group·interventional·Posted Jan 25, 2008·Updated Dec 30, 2019

In Brief

A Phase 3 clinical trial evaluating Bevacizumab and Paclitaxel and Bevacizumab and Capecitabine for Metastatic Breast Cancer. Completed, enrolled 564 participants across 55 sites in 12 countries.

Detailed Summary

First-line treatment of patients with locally recurrent or metastatic, HER2-negative breast cancer who have not received prior chemotherapy for locally recurrent or metastatic disease.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesAustria, Bosnia and Herzegovina, Bulgaria, Croatia, Czechia, Hungary, Israel, Latvia, Poland, Romania, Serbia, Slovakia
Collaborators--

Timeline

Phase 3CompletedFinished
20082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedJan 25, 2008
Enrollment StartApr 1, 2008
Primary CompletionSep 1, 2014
Study CompletionDec 1, 2014
TodayJul 2, 2026
Enrollment to primary: 6.4 yearsPosted 18.4 years ago

Interventions

Bevacizumab and Paclitaxelbiological

A: Bevacizumab 10 mg/kg i.v., days 1 and 15, every 4 weeks Paclitaxel 90 mg/m2, days 1, 8 and 15, every 4 weeks

Bevacizumab and Capecitabinebiological

B:Bevacizumab 15 mg/kg i.v., day 1, every 3 weeks Capecitabine twice-daily 1000 mg/m², day 1 to 14, every 3 weeks