Phase 2 Liver Cancer Trial, Recruiting NCT03897543 Sponsor: Abivax S.A. Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT03897543
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:

  • Adults aged 18 or older
  • People who are generally well enough to carry out daily activities with little or no limitation (as measured by a standard health scale called ECOG, score 0 or 1)
  • People who have been diagnosed with liver cancer (HCC) through a tissue sample, where surgery or local treatment to remove or destroy the cancer is not possible
  • People whose liver cancer was shown on scans to have grown or spread during or after local treatment, or after treatment with sorafenib or lenvatinib, or who were unable to tolerate or chose not to receive those medicines
  • People who have had at least one previous systemic (whole-body) treatment for liver cancer
  • People whose treating doctor determines they are suitable for treatment with nivolumab
  • People who have at least one area of cancer that can be measured on scans, using a standard method called RECIST v1.1
  • People whose liver is still functioning at a level called Child-Pugh class A, confirmed within 7 days before the first dose
  • People with no history of a condition called hepatic encephalopathy (confusion or brain problems caused by liver disease)
  • People with no significant fluid build-up in the abdomen (ascites) that requires a medical procedure to drain it — fluid visible only on scans but not causing symptoms may still be acceptable (confirm with trial site)
  • People with hepatitis B (HBV) infection who have been on antiviral treatment for at least 12 weeks and whose HBV virus levels are confirmed to be below 100 IU/mL within 7 days before the first dose
  • People who do not have an active simultaneous infection of both hepatitis B and hepatitis C, or both hepatitis B and hepatitis D
  • People with no current or recent problems with drug or alcohol misuse

Who may not be able to join:

  • People who have taken a type of cancer medicine called a tyrosine kinase inhibitor within 2 weeks before the first dose
  • People who have had bleeding from swollen veins in the oesophagus or stomach within the past 6 months
  • People whose liver cancer has grown into the main portal vein, the large vein returning blood to the heart (inferior vena cava), or the heart itself, as seen on scans
  • People who have previously had an organ or bone marrow/blood cell transplant
  • People who have an active autoimmune disease (where the immune system attacks the body) that has required ongoing medical treatment in the past 2 years
  • People who have been diagnosed with an immune system deficiency, or who have been taking steroid medicines or other immune-suppressing medicines within 7 days before the first dose
  • People who have had a local liver treatment or major liver surgery within 6 weeks before the first dose
  • People who have had minor surgery to the liver or anywhere else in the body within 1 week before the first dose

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 15 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

Principal Investigator: Darren SIGAL, MD, Scripps Clinic/Scripps MD Anderson Cancer Center

Phone: +33 153 830 961

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
Abivax S.A.
Registry
ClinicalTrials.gov
Start date
30 August 2019
Est. completion
30 June 2021

Where this trial is recruiting

🇺🇸 United States

Primary endpoints

Incidence of adverse events (AEs)

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: 15 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