16
Participants
Start Date
January 31, 2005
Primary Completion Date
November 30, 2008
Study Completion Date
November 30, 2008
Capecitabine
Participants will receive oral capecitabine, 1000 mg/m\^2 twice daily on Days 1 to 14 of each 21-day cycle, for at least 6 cycles (18 weeks). Treatment may continue until disease progression, intolerable toxicity, or consent withdrawal.
Peginterferon alfa-2a
Participants will receive SC peginterferon alfa-2a, 180 mcg every week during each 21-day cycle, for at least 6 cycles (18 weeks). Treatment may continue until disease progression, intolerable toxicity, or consent withdrawal.
Kueishan
Tainan City
Bangkok
Bangkok
Chiang Mai
Songkhla
Beijing
Guangzhou
Hoffmann-La Roche
INDUSTRY