10
Participants
Start Date
June 30, 2025
Primary Completion Date
June 30, 2027
Study Completion Date
June 30, 2028
Stapokibart and Finotonlimab
"Receive the combination of Stapokibart and Finotonlimab in cycles 1-3, and maintain treatment with Finotonlimab in subsequent cycles.~Stapokibart, 600mg for the first cycle, 300mg for the second and third cycles, administered subcutaneously every 3 weeks, for a total of 3 doses of Stapokibart; Finotonlimab 200mg, administered intravenously every 3 weeks until confirmed disease progression occurs according to the RECIST 1.1 imaging criteria (if the researcher determines that the subject can benefit from continuing PD-1 drug treatment, and the subject can tolerate the study treatment and agree, PD-1 drug can be continued and recorded in the study records), unacceptable toxic side effects, initiation of new anti-tumor treatment, withdrawal from the study or death (whichever occurs first), or reaching a maximum treatment period of 2 years."
Beijing Tongren Hospital, Capital Medical University, Beijing
Collaborators (1)
Keymed Biosciences Co.Ltd
INDUSTRY
Sinocelltech Ltd.
INDUSTRY
Beijing Tongren Hospital
OTHER