Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2026-03-26 @ 3:15 PM
Ignite Modification Date:
2026-03-26 @ 3:15 PM
NCT ID:
NCT07392866
Eligibility Criteria:
Inclusion Criteria:
* Subjects participate voluntarily and sign informed consent.
* Age ≥ 18 and ≤ 75 years old, male or female.
* Histological or clinical diagnosis of HCC.
* Barcelona Clinic Liver Cancer stage C. BCLC stage B, not suitable for radical surgery and/or local treatment
* Previous treatment with a drug containing an immune checkpoint inhibitor failed.
* Child-Pugh ≤7 , no history of hepatic encephalopathy.
Exclusion Criteria:
* Histologically documented fibrolamellar hepatocellular carcinoma, sarcoma-like hepatocellular carcinoma, etc.
* History of malignancy other than HCC within 5 years prior to the start of study treatment.
* History of liver transplantation, or planned to receive liver transplantation.
* Moderate or severe ascites with clinical symptoms that require drainage, uncontrolled or moderate or severe pleural and pericardical effusion.
* Has known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
* Involvement of both the main portal vein and the left and right branches by portal vein tumor thrombus, or of both the main trunk and the superior mesenteric vein concurrently, or of inferior vena cava.
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
75 Years
Study:
NCT07392866
Study Brief:
Protocol Section:
NCT07392866