338
Participants
Start Date
January 18, 2019
Primary Completion Date
March 25, 2024
Study Completion Date
March 25, 2024
AK104
Subjects will receive AK104 by intravenous administration.
Oxaliplatin
Subjects will receive AK104 in combination with oxaliplatin and capecitabine.
Capecitabine
Subjects will receive AK104 in combination with oxaliplatin and capecitabine.
Beijing Cancer Hospital, Beijing
Lead Sponsor
Collaborators (1)
Akeso Pharmaceuticals, Inc.
OTHER
Akeso
INDUSTRY