Liver Cancer Trial, Recruiting NCT06864481 Sponsor: University Hospital, Montpellier Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT06864481
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:

  • Adults aged 18 or older
  • People who are willing to take part in the study
  • People who have cancer and are receiving treatment before surgery (neoadjuvant), after surgery (adjuvant), or as ongoing maintenance treatment
  • People who are being treated with a type of cancer drug called an immune checkpoint inhibitor (ICI) — either on its own or combined with other cancer treatments such as targeted therapy, chemotherapy, or radiotherapy — whether as a first treatment or after previous treatment that included ICIs
  • People who have received at least one dose of an immune checkpoint inhibitor
  • People who have developed liver inflammation (hepatitis) after starting treatment, shown by specific blood test results being significantly above normal levels (confirm with trial site for exact values)
  • People whose liver inflammation is classified as severe (grade 3 or 4) according to standard medical grading

Who may not be able to join:

  • People whose liver inflammation has a cause other than their cancer treatment — for example, a viral infection, an autoimmune condition, reduced blood flow to the liver, heavy alcohol use, or a condition called Wilson's disease
  • People who are not able to communicate their agreement or non-objection to taking part
  • People who are in custody, under legal guardianship or curatorship, or in an emergency medical situation
  • People who are not covered by a social security or healthcare system (confirm with trial site regarding specific coverage requirements)

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 28 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

Phone: Phone: +33467330224

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
22 April 2025
Est. completion
22 April 2028

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Ratio cholestatic phenotype, cytolytic phenotype and mixed phenotype

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: 28 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