Trial statusNot yet recruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorThe Affiliated Hospital of Xuzhou Medical University
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
60 Participants
are divided into 1 treatment groupLocations
Sponsors and collaborators
Source ClinicalTrials.gov