Liver Cancer Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who have been diagnosed with hepatocellular carcinoma (a type of liver cancer) confirmed by imaging scans, tissue sample, or cell testing
- People whose liver cancer is classified as an advanced stage (BCLC Stage C), meaning the cancer has spread outside the liver and/or has grown into major blood vessels
- People who have not previously received any systemic (whole-body) treatment for their liver cancer, such as chemotherapy, targeted therapy, or immunotherapy
- People whose treatment included only commercially available (approved and marketed) checkpoint inhibitor drugs (PD-1/PD-L1 inhibitors) and anti-angiogenic drugs, though these do not need to be specifically approved for liver cancer
- People who received a procedure called TACE (a treatment delivered directly to the liver's blood vessels) either after starting the above drug combination, or up to 3 months before starting it
- People who received at least one full cycle of the combination drug therapy (PD-1/PD-L1 inhibitor plus anti-angiogenic drug) after the TACE procedure
- People who have measurable liver tumours that can be tracked on repeated imaging
Who may not be able to join:
- People whose liver cancer is a specific subtype, including cholangiocarcinoma, fibrolamellar, sarcomatoid hepatocellular carcinoma, or mixed hepatocellular/cholangiocarcinoma, as confirmed by tissue or pathology testing
- People whose treatment history does not fit the required timing described in the inclusion criteria
- People with severely reduced liver function (Child-Pugh Class C), a physical performance status score above 2, or severe brain complications related to liver disease (hepatic encephalopathy)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Gao- Teng, M.D, Zhongda hospital, Southeast university, Nanjing, China
Phone: +86-02583272121
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Overall Survival(OS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.