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New study aims to predict who will benefit from liver cancer immunotherapy

NCT ID NCT07623265

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at ways to personalize treatment for people with liver cancer (hepatocellular carcinoma). Researchers want to find out which patients are likely to respond to immunotherapy by testing their tumor tissue and blood before treatment starts. The goal is to avoid giving ineffective treatments and their side effects to those who won't benefit. About 300 adults with suspected or confirmed liver cancer will participate.

This is an AI summary of the original study and may miss details. Read our disclaimer.

Study facts

What this study's own registry entry says, in plain language.

Phase

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 300 people

The number the study aims to enrol. It can still change while the study runs.

Started

Mar 2025

Expected to finish

Jan 2032

An estimate. End dates often move.

Lead sponsor

Other sponsor

The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.

Who can take part

This study's own entry requirements. Only the study team can say for certain whether you qualify.

Ages

18 years and older

Sex

Anyone

Healthy volunteers

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

Show the full entry requirements

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

* General inclusion Criteria: 1. Male or female, age \> 18 years 2. Diagnosis or suspected diagnosis of hepatocellular carcinoma based on imaging * Specific inclusion criteria cohort 1 (retrospective/prospective data may be applicable): 1. Pathologically confirmed HCC 2. Treated with systemic treatment \[tyrosine kinase inhibitor (TKI) or immunotherapy (ICI)\] in the last 7 years and follow-up data (at least one imaging on treatment) available until 01/01/2025 3. Biopsy obtained between 01/01/2018 until 01/01/2025 4. Left-over tissue from previous diagnostic biopsies or resection specimens available 5. Time between biopsy and initiation of systemic treatment \< 1 year 6. Ability to sign informed consent for secondary use of archival tissue and data collection for study-specific research for patients who are alive * Specific inclusion criteria cohort 2 (aHCC \& prospective): 1. Suspicion of hepatocellular carcinoma (imaging criteria or recurrent disease of previously treated HCC) 2. Indication for tumor biopsy per standard of care 3. Eligible for systemic treatment (any) after pathological confirmation of HCC 4. Ability to sign informed consent for primary use of tissue and blood samples and data collection for study-specific research * Specific inclusion criteria cohort 3 (eHCC \& prospective): 1. Suspicion of hepatocellular carcinoma (imaging criteria or recurrent disease of previously treated HCC) 2. Indication for local treatment (resection or ablation) 3. Ability to sign informed consent for primary use of tissue and blood samples and for data collection for study-specific research Due to the observational nature of this study, participation in other (interventional) clinical trials is permitted, if biological materials can be collected per protocol. * General exclusion criteria: 1. Poor liver function and/or performance status which prohibits active treatment 2. Pathologically proven other malignancies of the liver, including primary cholangiocarcinoma or liver metastases 3. Treatment plan other than systemic treatment or local treatment (resection or ablation), such as TACE, TARE, liver transplantation

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Conditions

The condition(s) this trial relates to.

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    4 sites. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • AZ Delta

    RECRUITING

    Roeselare, Belgium

  • AZ Groeninge

    RECRUITING

    Kortrijk, Belgium

  • Jessa ziekenhuis

    RECRUITING

    Hasselt, Belgium

  • UZA

    RECRUITING

    Antwerp, Belgium

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