195
Participants
Start Date
August 31, 2010
Primary Completion Date
November 30, 2013
Study Completion Date
August 31, 2014
Capecitabine/Cisplatin + Sorafenib
Capecitabine 800 mg / m² po bid (D1-14) Cisplatin 60 mg / m² IV Day 1 Sorafenib 400 mg p.o. bid continuous dosing
Capecitabine/Cisplatin
Capecitabine 1000 milligram (mg) / m² po bid (D1-14) Cisplatin 80 mg / m² IV Day 1
Asan Medical Center, Seoul
Lead Sponsor
Collaborators (1)
Bayer
INDUSTRY
Asan Medical Center
OTHER