40
Participants
Start Date
March 31, 2024
Primary Completion Date
March 31, 2026
Study Completion Date
March 31, 2027
Cadonilimab+regorafenib
cadonilimab: 6mg/kg iv D1 Q2W; regorafenib: 80mg QD oral; Eligible patients will receive cadonilimab combined with regorafenib, until disease progression or intolerable toxicity or death or withdrawal of informed consent, whichever occurred first
RECRUITING
Mengchao Hepatobiliary Hospital, Fujian Medical University, Fuzhou
Meng Chao Hepatobiliary Hospital of Fujian Medical University
OTHER