28
Participants
Start Date
January 9, 2006
Primary Completion Date
July 8, 2008
Study Completion Date
July 8, 2008
S-1
All participants received S-1 orally at a dose of 30 mg/m2 BID for 14 days followed by a 1-week recovery period, repeated every 3 weeks. The trial was planned to proceed to the second stage only if sufficient efficacy was demonstrated in Stage 1.
Quintiles, Inc.
INDUSTRY
United BioSource, LLC
INDUSTRY
Taiho Oncology, Inc.
INDUSTRY