8
Participants
Start Date
April 2, 2024
Primary Completion Date
November 30, 2025
Study Completion Date
November 30, 2025
T3011 hepatic artery infusion
The study was divided into two dose groups, T3011 3×10\^8 PFU/time (HAI) and T3011 1×10\^9 PFU/time (HAI), with a 3+3 dose escalation design. After the completion of the lead-in period, the patient entered the combination therapy period(combination therapy with T3011 hepatic artery infusion , Regorafenib and Toripalimab),and the dosage of T3011 was determined according to the safety observation results of the lead-in period, the dose of toripalimab was 80mg intravenously, and regorafenib was 80mg orally once a day.
toripalimab
The combination therapy period: toripalimab, 80mg intravenous ,D2 and D16, 4 weeks per cycle
regorafenib
The combination therapy period: regorafenib ,80mg orally once a day, D1-D21,4 weeks per cycle
Immvira Co., Limited
UNKNOWN
China Medical University, China
OTHER