drugset / Trial / NCT00476827

A Phase II Safety and Tolerability Study of Bevacizumab When Added to Single-agent Chemotherapy to Treat Patient With Breast Cancer Metastatic to Brain

NCT00476827

Phase 2 Terminated 16 enrolled Duke University Genentech, Inc. · collab
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Our hypothesis is that this study design, in which bevacizumab is added to one of six single agent chemotherapies with proven activity in metastatic breast cancer, will result in regression or stabilization of this disease in a safe and tolerable manner.

Timeline

Start
2007-05
Primary completion
2011-05
Completion
2011-05

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bevacizumab Monoclonal antibody 10 mg/kg Intravenous
Comparator Bevacizumab Monoclonal antibody 15 mg/kg Intravenous
Comparator Docetaxel Small molecule 35 mg/m2 Intravenous
Comparator Gemcitabine Small molecule 1000 mg/m2 Intravenous
Comparator Irinotecan Small molecule 125 mg/m2 Intravenous
Comparator Irinotecan Small molecule 340 mg/m2 Intravenous
Comparator Paclitaxel Small molecule 90 mg/m2 Intravenous
Comparator Vinorelbine Small molecule 25 mg/m2 Intravenous

Indications