12
Participants
Start Date
January 31, 2008
Primary Completion Date
July 31, 2009
Study Completion Date
March 31, 2010
sunitinib + mFOLFOX6
37.5 mg/day, oral, administered on an outpatient basis for 4 weeks on, 2 weeks off (Schedule 4/2)
sunitinib + mFOLFOX6
50 mg/day, oral, administered on an outpatient basis for 2 weeks on, 2 weeks off (Schedule 2/2)
Pfizer Investigational Site, Kashiwa
Pfizer Investigational Site, Suntougun
Pfizer Investigational Site, Chuo-ku
Lead Sponsor
Pfizer
INDUSTRY