60
Participants
Start Date
May 21, 2024
Primary Completion Date
December 31, 2025
Study Completion Date
December 31, 2027
AK104+Axitinib
Subjects receive AK104 10mg/kg intravenously (IV) every 3-week cycle plus Axitinib until progression.
AK112+Axitinib
Subjects receive AK112 20mg/kg intravenously (IV) every 3-week cycle plus Axitinib until progression.
Beijing Cancer Hospital, Beijing
Peking University Cancer Hospital & Institute
OTHER