Phase 2 Liver Cancer Trial, Recruiting NCT06478719 Sponsor: Febico Biomedical Corp. Condition: Liver Cancer
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Phase 2 Liver Cancer Trial, Recruiting

NCT06478719
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:

  • People aged 18 to 75 years of any gender
  • People who are willing and able to give written consent to participate
  • People who have a confirmed diagnosis of liver cancer (hepatocellular carcinoma), confirmed by imaging, tissue sample, or cell sample
  • People who are willing to undergo a procedure called TACE (a treatment that delivers medicine directly to liver tumours through the blood vessels)
  • People who are generally well enough to carry out light activity and care for themselves (a measure doctors use called ECOG performance status of 0–1)
  • People who are expected to live for more than 3 months
  • People whose blood test results at the screening visit fall within specific ranges for liver enzymes, blood clotting, blood cell counts, bilirubin, and kidney function (confirm with trial site for exact values)
  • People whose liver shows a certain level of stiffness on a specialist liver scan, indicating some degree of liver scarring or fibrosis (confirm with trial site)

Who may not be able to join:

  • People whose cancer has spread into major blood vessels of the liver
  • People whose cancer has spread to areas outside the liver
  • People for whom the TACE procedure would be considered medically unsuitable by the treating doctors
  • People with acute liver failure or signs that the liver is no longer functioning adequately, such as confusion caused by liver disease or significant fluid build-up in the abdomen
  • People with active hepatitis B or C infection who are recommended to receive antiviral treatment (for example, people with hepatitis B virus levels of 20,000 IU/mL or higher, or detectable hepatitis C virus in their blood)
  • People with serious disease affecting the heart, lungs, brain, kidneys, or digestive system, as judged by the trial doctors
  • People with chronic pancreatitis (long-term inflammation of the pancreas)
  • People who are taking certain medications that could interfere with the trial (confirm with trial site for the specific list)
  • People who are unable to communicate their symptoms or health concerns, for example due to psychosis or severe neurological conditions
  • People who have had an active infection requiring antibiotics within the 4 weeks before their screening visit

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 9 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: Kai-Wen Huang, MD, MS, PhD, National Taiwan University Hospital

Phone: 886-2-2627-5585

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
Febico Biomedical Corp.
Registry
ClinicalTrials.gov
Start date
24 June 2024
Est. completion
7 June 2027

Where this trial is recruiting

🇹🇼 Taiwan

Primary endpoints

Changes in the level of liver function

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: 9 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