40
Participants
Start Date
May 31, 2005
Primary Completion Date
October 31, 2007
Study Completion Date
April 30, 2008
5-Fluorouracil
Intravenous 5-fluorouracil based chemotherapy will be administered until disease progression or until termination of the study. The chemotherapy regimen will be at the discretion of the prescriber and will not be provided by the sponsor.
Bevacizumab
Bevacizumab will be administered IV 5 mg/kg every 2 weeks until disease progression or until termination of the study.
Irinotecan
Irinotecan will be administered at the discretion of the prescriber until disease progression or until termination of the study.
Oxaliplatin
Oxaliplatin will be administered at the discretion of the prescriber until disease progression or until termination of the study.
Taipei
Taichung
Taichung
Chai Yi
Tainan City
Tainan City
Kaohsiung City
Kaohsiung City
Hoffmann-La Roche
INDUSTRY