About this trial
Evaluation of the efficacy and safety of Iparomlimab and Tuvonralimab Injection (QL1706) in combination with bevacizumab for postoperative adjuvant treatment of HCC with high-risk recurrence risk
Eligibility criteria
Qualifiers
Voluntarily participate in this study and sign the informed consent form;
Age 18-100 years old, male or female;
Hepatocellular carcinoma confirmed by histopathology, cytology or imaging;
CNLC PHASE I-II;
Disqualifiers
It is known that there are fibrotic plate HCC, sarcomatoid HCC or mixed-type cholangiocarcinoma and HCC;
There is evidence of residual, recurrent or metastatic disease;
History of hepatic encephalopathy;
Previous receipt of allogeneic stem cell or solid organ transplantation, or on the waiting list for liver transplantation;
Trial design
Treatments tested in this trial
- Iparomlimab and Tuvonralimab Injection (QL1706) plus bevacizumab
Treatment groups
Locations
Sponsors and collaborators
The Affiliated Hospital of Xuzhou Medical University
Lead sponsor