Phase 2 Liver Cancer Trial, Recruiting NCT06742424 Sponsor: West China Hospital Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT06742424
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 who have been diagnosed with hepatocellular carcinoma (a type of liver cancer), either confirmed through a tissue sample or through standard clinical diagnosis methods
  • People whose liver cancer has spread outside the liver (metastases) and cannot be removed with surgery, as confirmed by imaging scans
  • People who have not previously been treated with a PD-L1 antibody medicine or bevacizumab (specific types of cancer treatments)
  • People aged 18 to 75 years
  • People with a general health and activity level rated as 0 or 1 on a standard medical scale, meaning they are fully active or have only minor limitations in physical activity
  • People with liver function rated as Child-Pugh Class A or B7 (a standard measure of how well the liver is working)
  • People who are willing and able to follow all the requirements of the study
  • People who have at least one measurable or assessable area of cancer visible on scans, according to standard measurement guidelines
  • People whose blood counts and organ function meet minimum levels, including sufficient white blood cells, platelets, haemoglobin, and acceptable kidney, liver, and thyroid function (confirm specific values with trial site)
  • People with a life expectancy of at least 12 weeks
  • People of childbearing potential who are willing to use effective contraception during treatment and for 6 months after the last dose

Who may not be able to join:

  • People who have serious complications from liver disease, such as severe bleeding, active infection, or confusion caused by liver failure
  • People who have previously had any systemic (whole-body) treatment for their liver cancer
  • People who have had another cancer within the past 5 years, except for certain treated skin cancers or early-stage cancers that have been fully treated
  • People who are currently taking part in another interventional clinical trial
  • People who have used Chinese herbal medicine or immune-modifying treatments within 2 weeks before the first dose
  • People who have an active autoimmune disease that has required systemic treatment within the past 2 years
  • People who have used systemic corticosteroid medicines (such as prednisone) within 7 days before the first dose
  • People who have previously had an organ transplant (other than a cornea transplant) or a stem cell transplant
  • People with a known allergy to monoclonal antibody medicines or to any components used in the treatment being studied
  • People who have not sufficiently recovered from side effects of previous treatments
  • People with a known HIV infection
  • People with an untreated active hepatitis B infection (confirmed by specific blood test results)
  • People with an active hepatitis C infection
  • People who have received a live vaccine within 30 days before the first dose
  • People who are pregnant or breastfeeding
  • People with serious or uncontrolled health conditions, including certain heart problems, uncontrolled high blood pressure, a blood clot or arterial event in the past 6 months, active lung disease, active tuberculosis, active serious infections, uncontrolled diabetes, significant kidney protein leakage, psychiatric conditions that may affect participation, or any other condition that could interfere with the study (confirm specific conditions with trial site)

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 23 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.

Contact this trial

Phone: +8613281003787

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

Status
Recruiting
Phase
Phase 2
Sponsor
West China Hospital
Registry
ClinicalTrials.gov
Start date
1 October 2024
Est. completion
30 April 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Objective Response Rate (ORR) as Assessed by RECIST v1.1

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: 23 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