Liver Cancer Trial, Recruiting NCT05911633 Sponsor: Terumo Europe N.V. Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT05911633
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:

  • You are at least 18 years old
  • You have been diagnosed with liver cancer (HCC) confirmed by a tissue sample or by standard European liver disease guidelines
  • Your tumor(s) are smaller than 5 cm, and the total of your largest tumor's size (in cm) plus the number of tumors you have adds up to 7 or less
  • Your liver cancer is at an early or intermediate stage (BCLC Stage A or B) and curative treatment is not currently an option for you
  • Your cancer has come back or your previous surgery or ablation treatment did not fully work — this is allowed, unless the cancer has returned in the exact area where a heat-based (thermal) ablation was previously done
  • You are generally active and able to carry out daily activities with little or no limitation (performance status 0 or 1)
  • Your cancer can be treated in a single session at the start of the trial
  • Your liver is either healthy or has stable, well-controlled scarring (cirrhosis) with good liver function (Child-Pugh Class A)
  • Your bilirubin level (a liver marker in your blood) is within an acceptable range
  • Your blood counts — including red blood cells, white blood cells, and platelets — meet the minimum required levels
  • You have no fluid build-up in your abdomen, or only a small amount that is managed by reducing salt in your diet (not by water tablets or drainage procedures)
  • Your kidneys are working well enough as shown by blood test results
  • You are willing and able to sign a consent form agreeing to take part
  • If you are able to have children, you agree to use reliable contraception throughout the study and during follow-up

Who may not be able to join:

  • You have previously had any systemic (whole-body) drug treatment for your liver cancer
  • You have previously had any treatment delivered directly into the arteries of your liver (intra-arterial therapy) for liver cancer
  • You are currently eligible for a curative treatment for your liver cancer
  • Your cancer has returned in the same area where a previous heat-based (thermal) ablation was performed
  • Your liver disease is at an advanced stage, or you have had internal bleeding from your digestive system or confusion caused by liver failure
  • Your liver cancer is at an advanced stage (BCLC Class C or D), has spread into blood vessels or outside the liver, or is causing significant symptoms
  • You have a history of another type of cancer, unless it was fully treated at least 5 years ago with no signs of it returning, or it occurred more recently but is not active and is not expected to come back or cause problems within the next 5 years
  • You have a history of bile duct disease or blockage
  • You have blood clots in the portal vein, abnormal blood flow patterns in your liver, or absent blood flow in the part of the liver being treated
  • You are unable to have CT or MRI scans with contrast dye — for example, due to an allergy to contrast materials
  • You have any other medical reason that would prevent you from safely having the embolization procedure or the chemotherapy drug (Doxorubicin) used in this trial
  • You are currently taking part in another clinical trial involving an experimental drug or device that may interfere with this study
  • Your doctor feels that other health conditions you have could affect your ability to safely participate or complete the study (confirm with trial site)
  • You are pregnant or currently breastfeeding

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 26 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: Marie-Pierre Dewez, Terumo Europe EMCD

Phone: +32 483 53 41 06

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
Sponsor
Terumo Europe N.V.
Registry
ClinicalTrials.gov
Start date
27 February 2024
Est. completion
30 September 2026

Where this trial is recruiting

🇧🇪 Belgium 🇫🇷 France 🇩🇪 Germany 🇮🇹 Italy

Primary endpoints

Safety: by evaluating all procedural or study device related grade 3-4-5 adverse events (AEs); Technical success

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: 26 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