30
Participants
Start Date
October 31, 2005
Primary Completion Date
March 31, 2009
Study Completion Date
April 30, 2011
Avastin
All patients will received Avastin 15 mg/kg IV every three weeks. The first evaluation will be done at Week 6. Patients with objective response or stable disease will continue therapy with restaging every 6 weeks until evidence of disease progression. Patients with progression of disease will be taken off study.
Hormonal therapy
aromatase inhibitor (letrozole 2.5mg/d PO, anastrazole 1mg/d PO, or exemestane 25mg/d PO)or Selective Estrogen Receptor Modulator (SERM) (tamoxifen 20mg/d PO)
University of Alabama at Birmingham, Birmingham
Collaborators (1)
Genentech, Inc.
INDUSTRY
University of Alabama at Birmingham
OTHER