Phase 2 Liver Cancer Trial, Recruiting NCT07246668 Sponsor: Yonsei University Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT07246668
Recruiting Phase 2

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 hepatocellular carcinoma (a type of liver cancer) confirmed by biopsy or imaging, at a stage classified as BCLC B or C, where curative surgery or a liver transplant is not an option
  • People who have at least one tumour that can be measured on scans according to standard criteria (called RECIST)
  • People whose treating doctor has determined them suitable for a combination of two medicines: atezolizumab and bevacizumab
  • People whose radiation specialist has assessed them as a candidate for a specialised type of radiation treatment called carbon ion radiotherapy
  • People whose liver is functioning at a level classified as Child-Pugh class A (a measure of liver health)
  • People with a general health and activity level rated as ECOG 0 or 1 (meaning largely or fully active day-to-day)
  • People whose blood counts and organ function meet specific minimum levels, including white blood cells, platelets, haemoglobin, kidney function, liver enzyme levels, and bilirubin
  • People who either have no uncontrolled varicose veins in the oesophagus or stomach (confirmed by a camera test within the past 6 months), or have had those veins adequately treated before joining
  • People who are willing and able to read, understand, and sign a consent form for the study

Who may not be able to join:

  • People who have received certain cancer medicines (anti-PD-1, anti-PD-L1, or anti-VEGF therapies) within the past year
  • People who have previously had carbon ion radiotherapy to the same area of the body being treated
  • People with serious or uncontrolled heart conditions, including a heart attack within the past 6 months, uncontrolled high blood pressure, or severe heart failure (NYHA class III or IV)
  • People with an active autoimmune disease (where the immune system attacks the body) that requires ongoing medication to suppress the immune system, or a history of such a condition
  • People with an active, uncontrolled infection, including bacterial, viral, or fungal infections, active tuberculosis, HIV, or hepatitis B or C with viral levels that are not under control
  • People with a significant risk of bleeding, including active gastrointestinal bleeding, untreated or high-risk varicose veins in the digestive tract, or a blood-clotting problem that cannot be managed with standard treatment
  • People with a specific type of blood clot in the main vein of the liver (portal vein tumour thrombosis, grade Vp4) that the study doctor considers unsuitable for treatment
  • People who are pregnant or breastfeeding
  • People who have previously had any organ transplant, including a liver transplant
  • People with any other condition that the study doctor considers likely to affect safe or full participation in 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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 27 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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Trial details

Status
Recruiting
Phase
Phase 2
Registry
ClinicalTrials.gov
Start date
10 March 2025
Est. completion
1 March 2027

Where this trial is recruiting

🇰🇷 South Korea

Primary endpoints

Progression-Free Survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov