30
Participants
Start Date
September 19, 2024
Primary Completion Date
August 1, 2026
Study Completion Date
August 1, 2027
Cadonilimab+S-1or Capecitabine
Eligible patients will receive Cadonilimab (6mg/k, iv, D1,Q3W)combined with S-1 (40-60mg po BID Q3W D1-14)or Capecitabine (1250mg/m2, po BID Q3W D1-14)until disease progression or unacceptable toxicity. Patients who had used S-1 in the first line should choose capecitabine; patients who had used capecitabine in the first line should choose S-1; otherwise decided by investigator's choice.
RECRUITING
Shanghai General Hospital, Shanghai
Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine
OTHER