23
Participants
Start Date
October 1, 2025
Primary Completion Date
December 31, 2029
Study Completion Date
December 31, 2030
Anlotinib and Benmelstobart
Patients will receive Benmelstobart (1200mg, d1, q3w) in combination with Anlotinib (12mg, qd, d1-14, q3w). Treatment will continue until disease progression, voluntary withdrawal of informed consent, intolerable toxicity, or until the investigator determines that the patient no longer benefits.
Fudan University
OTHER