New study tracks immune therapy results in advanced liver cancer
NCT ID NCT07321067
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study will follow 75 adults with advanced liver cancer who are already receiving immune checkpoint inhibitors as part of their regular care. Researchers will track how long patients live and how long the cancer stays under control. The goal is to better understand the real-world effectiveness of these treatments.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- immune checkpoint inhibitors (e.g., atezolizumab-bevacizumab, durvalumab-tremelimumab)
- What this could lead to
- If successful, this study could provide real-world data on how well these drugs work for advanced liver cancer, helping guide future treatment decisions.
- What could go wrong
- This is an observational study, not a controlled trial. Results may be limited by small size (75 people) and lack of a comparison group.
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.
- Participants
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About 75 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jan 2026
An estimate. Start dates often move.
- Expected to finish
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Nov 2027
An estimate. End dates often move.
- Lead sponsor
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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.
Who is studied
patients diagnosed with advanced hepatocellular carcinoma either denovoor after prior line of treatment
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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 Hide 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.
Inclusion Criteria: * Adults (≥18 years) with radiologically or histologically confirmed advanced HCC * Candidates for systemic immune checkpoint inhibitors (e.g., atezolizumab-bevacizumab, durvalumab-tremelimumab). * Patients with preserved liver function. ( up to G2 using ALBI score or up to B (7 ) using Child-Pugh socring system) . Exclusion Criteria: * Child-Pugh C liver function. * Prior liver transplantation. * patients with concurrent malignancies other than HCC. * Active autoimmune disease requiring systemic immunosuppression.
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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.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Sohag university hospitals
Sohag, Sohag Governorate, 82511, Egypt
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sSohag oncology centre
Sohag, Sohag Governorate, 82511, Egypt
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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