635
Participants
Start Date
January 31, 2007
Primary Completion Date
September 30, 2013
Study Completion Date
December 31, 2013
capecitabine + bevacizumab
Ca 1250 mg/m2 daily orally continuously, B 7.5 mg/kg i.v. q 3 w
observation
observation after induction treatment
University Medical Center Nijmegen, Nijmegen
Collaborators (1)
Koningin Wilhelmina Fonds
OTHER
Sanofi
INDUSTRY
Hoffmann-La Roche
INDUSTRY
Dutch Colorectal Cancer Group
OTHER