36
Participants
Start Date
September 1, 2025
Primary Completion Date
September 1, 2027
Study Completion Date
September 1, 2027
SHR-1701
SHR-1701 will be administered by IV, 1200mg on day 1 of each 21 day cycle until documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent.
Famitinib
Famitinib will be administered at 15 mg orally daily until documented disease progression, development of unacceptable toxicity, participant request, or withdrawal of consent.
Cryoablation
Cryoablation will be performed with a two-cycle freeze-thaw phase protocol; US or non-contrast CT images will be obtained to visualize the evolving ablation zone. SHR-1701 plus famitinib will be administered 1-3 days after cryoablation.
Zhongshan Hospital, Fudan University, Shanghai
Fudan University
OTHER