Phase 2 Liver Cancer Trial, Recruiting NCT05528952 Sponsor: Centre Hospitalier Universitaire de Besancon Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT05528952
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 signed an informed consent form agreeing to take part in the study
  • People whose liver cancer has been confirmed through a tissue sample (biopsy)
  • People whose cancer has spread, cannot be surgically removed, or is considered locally advanced
  • People who have not previously received any systemic (whole-body) anti-cancer treatment
  • People aged 18 years or older
  • People whose cancer can be measured using specific imaging guidelines (mRECIST criteria), including in some cases areas that were previously treated with radiation if the cancer has clearly grown back there
  • People who have previously had chemoembolization, radioembolization, or radiotherapy and have largely recovered from any side effects of those treatments (confirm with trial site for specific recovery requirements)
  • People with a reasonably good general level of physical functioning, as measured by a standard medical performance scale (confirm with trial site)
  • People whose liver is still functioning at a certain level, known as Child-Pugh Class A (confirm with trial site)
  • People whose liver cancer falls into a specific stage category (BCLC Stage C, or BCLC Stage B where local treatment is not considered appropriate) according to a standard liver cancer staging system

Who may not be able to join:

  • People who have previously received certain types of immunotherapy treatments targeting PD-1, PD-L1, CTLA-4, or any other immune-based cancer therapy
  • People who have been diagnosed with another cancer in the past 3 years, unless it was a skin cancer (basal cell type) or an early-stage cervical or breast cancer that was fully treated and removed
  • People with a medical or psychiatric condition that the treating doctor considers would make participation in the trial unsuitable
  • People who are currently taking part in another clinical trial or are within an exclusion period from a previous trial
  • People who are under legal guardianship or a similar form of legal protection
  • People with specific rare subtypes of liver cancer, including fibrolamellar HCC, sarcomatoid HCC, or a mixed liver and bile duct cancer
  • People with uncontrolled fluid build-up around the lungs or heart, uncontrolled fluid in the abdomen, or a symptomatic abnormal body passage (fistula)
  • People with cancer pain that is not well controlled and requires repeated hospitalisations or high-dose steroid treatment (treatable lesions should be treated with radiotherapy before joining)
  • People with active cancer that has spread to the brain or the lining of the brain, unless previously treated and confirmed to be stable
  • People with a history of brain confusion caused by liver disease (hepatic encephalopathy)
  • People who have had a bleeding episode from untreated or incompletely treated swollen veins in the oesophagus or stomach in the past 6 months
  • People with inadequate organ function, including serious heart conditions, unstable coronary artery disease, respiratory failure, uncontrolled infection, or another life-threatening condition

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 19 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: +33 3 81 47 99 99

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
Centre Hospitalier Universitaire de Besancon
Registry
ClinicalTrials.gov
Start date
27 September 2022
Est. completion
27 March 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

objective response rate (ORR)

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: 19 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