60
Participants
Start Date
February 28, 2005
Primary Completion Date
October 31, 2006
Study Completion Date
July 31, 2007
S-1
All patients will receive S-1 orally at a dose of 25 mg/m2 twice daily (BID) for 14 days followed by a 1-week recovery period, repeated every 3 weeks. The study may go to the third stage only if 7/31 (23%) or more patients have achieved a confirmed response (CR or PR) in stages 1 and 2 combined.
Quintiles, Inc.
INDUSTRY
United BioSource, LLC
INDUSTRY
Taiho Oncology, Inc.
INDUSTRY