55
Participants
Start Date
October 1, 2023
Primary Completion Date
October 1, 2024
Study Completion Date
October 1, 2027
Nimotuzumab、Tislelizumab
Subjects will receive Nimotuzumab 400 mg/time, intravenous injection, qw; Tislelizumab 200 mg/time, q3w until disease progression, intolerable toxicity, or 24 months of medication
Peking Union Medical College Hospital
OTHER