Liver Cancer Trial, Recruiting NCT05263830 Sponsor: Assistance Publique - Hôpitaux de Paris Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT05263830
Recruiting Not Applicable

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 to 89 years old
  • People diagnosed with liver cancer (called hepatocellular carcinoma, or HCC) that developed alongside a chronic liver condition or scarring of the liver (cirrhosis), regardless of the underlying cause, diagnosed according to specific French medical guidelines updated in June 2021
  • People for whom a specialist team meeting has agreed that a combination treatment called Atezolizumab and Bevacizumab is the appropriate systemic (whole-body) treatment, in line with current cancer society recommendations
  • People who understand the French language
  • People who have been informed about the study and have agreed to take part

Who may not be able to join:

  • People living with HIV, a known immune system deficiency, or those taking medications that suppress the immune system
  • People with autoimmune diseases (conditions where the immune system attacks the body) or those receiving other types of immunotherapy treatments
  • People who have previously had a liver transplant or a procedure to redirect blood flow around the liver (called a portosystemic shunt)
  • People who have a serious blood infection (sepsis) or who are taking medications to raise dangerously low blood pressure (vasoconstrictors)
  • People who are pregnant or breastfeeding
  • People who are legally under guardianship or have a legal curator managing their affairs

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 13 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Principal Investigator: Manon ALLAIRE, Dr, Assistance Publique - Hôpitaux de Paris

Phone: 0142161034

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
Not Applicable
Registry
ClinicalTrials.gov
Start date
8 September 2023
Est. completion
8 September 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

evaluate concentration of circulating GPC-3

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: 13 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