77
Participants
Start Date
May 31, 2005
Primary Completion Date
July 31, 2008
Study Completion Date
July 31, 2008
SU011248; Capecitabine
Dose finding study using SU011248 daily by oral capsule in a continuous regimen or administered for 4 out of every 6 weeks (Schedule 4/2) or 2 out of every 3 weeks (Schedule 2/1), with capecitabine administered 2 out of every 3 weeks until progression or unacceptable toxicity.
Pfizer Investigational Site, Nashville
Pfizer Investigational Site, Indianapolis
Pfizer Investigational Site, Albuqurque
Lead Sponsor
Pfizer
INDUSTRY