Phase 1 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 aged 18 or older
- People who have been diagnosed with advanced liver cancer (hepatocellular carcinoma), confirmed by tissue testing, cell testing, or medical assessment
- People whose liver cancer has been staged as Barcelona stage B or C (a system doctors use to assess how far the cancer has progressed)
- People who have not yet received any systemic (whole-body) treatment for their liver cancer
- People who have at least one tumour that can be measured using standard imaging guidelines
- People whose liver function scores fall within a certain range (Child-Pugh score A or B7 — confirm with trial site)
- People with a physical functioning score of 0 or 1 on the ECOG scale, meaning they are fully active or have only minor limitations in daily activities
- People whose doctors estimate they are likely to live for at least 12 weeks
- People whose major organs (such as heart, kidneys, and bone marrow) are functioning adequately
- People who have signed the trial's consent form
Who may not be able to join:
- People whose tissue or cell testing confirms certain less common types of liver or bile duct cancers, including mixed liver-bile duct cancer, sarcomatoid liver cancer, or fibrolamellar liver cancer
- People who have had, or currently have, another active cancer (other than liver cancer) within the past 5 years — though some fully treated localised cancers (such as certain skin, bladder, prostate, cervical, or breast cancers) may still be eligible (confirm with trial site)
- People who have previously received an organ transplant from another person, such as a liver transplant
- People whose liver tumours currently make up more than 50% of the total liver volume
- People who experienced significant bleeding (grade 3 or above) within the past 6 months, or moderate non-gastrointestinal bleeding (grade 2) within the past 3 months
- People who had an abdominal fistula, a hole in the gastrointestinal tract, or an abdominal abscess within the past 6 months
- People who had a major blood vessel problem within the past 6 months
- People who currently have, or have previously needed hormone treatment for, a lung condition involving scarring or inflammation of lung tissue (interstitial lung disease)
- People with a weakened immune system, whether from birth or due to a condition such as HIV infection
- People who had a serious infection within the 28 days before starting the trial
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
Phone: +86-0518-82342973
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
Trough serum concentrations (C21d); Area under curve from Day 0 to Day 21 (AUC0-21d); Area under curve up to 21 weeks (AUC0-21weeks)
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.