36
Participants
Start Date
July 31, 2005
Primary Completion Date
June 30, 2008
Study Completion Date
July 31, 2010
Bevacizumab
5 mg/kg IV
Cetuximab
400 mg/m2 (first cycle only) IV on day 1 and 250 mg/m2 IV on day 8 with all subsequent cycles 250 mg/m2 IV on days 1 and 8
5-fluorouracil
400 mg/m2 bolus IV bolus followed by 2400 mg/m2 administered as continuous IV infusion over 46 hours via pump (outpatient)
Leucovorin
350 mg IV
Oxaliplatin
85 mg/m2 IV
Center for Cancer and Blood Disorders, Bethesda
Tennessee Oncology, Nashville
Chattanooga Oncology and Hematology Associates, Chattanooga
Jackson Oncology Associates, Jackson
Consultants in Blood Disorders and Cancer, Louisville
Oncology Hematology Care, Cincinnati
Oncology Hematology Associates of SW Indiana, Evansville
St. Louis Cancer Care, Chesterfield
Methodist Cancer Center, Omaha
Mercy Hospital, Portland
Collaborators (1)
Bristol-Myers Squibb
INDUSTRY
SCRI Development Innovations, LLC
OTHER