Liver Cancer Trial, Recruiting NCT05398380 Sponsor: Hospital Vall d'Hebron Condition: Liver Cancer
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Liver Cancer Trial, Recruiting

NCT05398380
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 who are willing and able to sign a written consent form agreeing to take part in the study.
  • People aged between 18 and 70 years old at the time of joining the study.
  • People who are generally well or have only mild limitations in daily activity, as measured by a standard cancer fitness scale (ECOG score of 0 or 1).
  • People whose colorectal cancer has been confirmed by a tissue biopsy (laboratory test on a tumour sample).
  • People whose colorectal cancer has spread to both sides of the liver only, cannot be surgically removed, and this has been agreed upon by a team of medical specialists.
  • People who have already had their primary (original) colorectal tumour surgically removed following standard cancer surgery guidelines, with an appropriate cancer stage recorded.
  • People for whom at least 12 months have passed since their original colorectal tumour was removed.
  • People whose original tumour was at a certain stage of spread (stage T3N1 or lower). If more than 2 years have passed since the original tumour was removed, people with a slightly more advanced tumour stage (T4N0 or T4N2) may also be considered (confirm with trial site).
  • People who show no signs of cancer spread outside the liver, confirmed by specialised scans (PET/CT scan, CT scan, and pelvic MRI).
  • People who have received chemotherapy treatment for at least 3 months, and no more than two different chemotherapy regimens containing a specific type of drug (fluoropyrimidine-based), which may have been combined with other chemotherapy medicines or targeted therapies.
  • People whose liver tumours have remained stable or have partially shrunk during treatment, based on standard medical measurement guidelines, with this assessed at least 3 months after the most recent treatment and just before entering the study.
  • People whose blood level of a cancer marker called CEA is 80 µg/L or below, measured just before entering the study.
  • People whose blood test results show kidneys, platelets, and infection-fighting white blood cells are all functioning within acceptable ranges for this study.
  • People who experienced liver problems after their original surgery due to an underestimation of usable liver volume may still be considered, provided they meet all inclusion criteria and none of the exclusion criteria (confirm with trial site).

Who may not be able to join:

  • People whose largest liver tumour measures more than 5.5 cm just before entering the study.
  • People who have Lynch Syndrome, an inherited condition that increases cancer risk.
  • People whose cancer has a specific genetic change called a BRAF mutation, or whose original tumour showed a feature called microsatellite instability (MSI).
  • People whose original colorectal cancer has come back, confirmed by a camera examination of the bowel (colonoscopy) or pelvic MRI within the 12 months before entering the study.
  • People who have had another cancer within the past 5 years. People whose previous cancer was fully cured more than 5 years ago, or who had a type of skin cancer called basal cell carcinoma that was treated, may still be considered.
  • People with substance use issues, or medical, psychological, or social circumstances that could affect their ability to take part in or complete the study.
  • People with uncontrolled heart or lung conditions that would make any surgical procedure unsafe.
  • People with an active infection at the time of joining.
  • People who are pregnant or currently breastfeeding.
  • People whom the medical team running the trial considers unsuitable to participate, for any reason.

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 22 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: Ramón Charco, Department of HPB Surgery and Transplants, Hospital Universitario Vall d´Hebron

Phone: +34932746113

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
Hospital Vall d'Hebron
Registry
ClinicalTrials.gov
Start date
1 January 2022
Est. completion
31 December 2026

Where this trial is recruiting

🇪🇸 Spain

Primary endpoints

Five years overall survival

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: 22 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