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NCT07321067Not yet recruiting

Use of Immune Checkpoint Inhibitors in Patients With Advanced Hepatocellular Carcinoma : Efficacy and Outcomes

Source: ClinicalTrials.gov · Last updated 6 Jan 2026

Brief summary (registry, in English)

the Objectives of this study are: • Primary Objective: To prospectively evaluate overall survival (OS), ICI-specific survival (OS-ICI), and progression-free survival (PFS) in patients with advanced HCC treated with immune checkpoint inhibitors. the main question it aims to answer is: What are the clinical outcomes (overall survival, progression-free survival, and OS-ICIs) of immune checkpoint inhibitor therapy in patients with advanced hepatocellular carcinoma? Participants already taking immune checkpoint inhibitors as part of their regular medical care.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
75 (estimated)
First submitted
21 Dec 2025
Start date
1 Jan 2026
Primary completion date
1 Nov 2026
Lead sponsor
Ahmed Karam Helmy
NCT number
NCT07321067

What you commit to

  • Study type: Observational
  • Planned participants: 75
  • From 1 Jan 2026 to the primary completion date, 1 Nov 2026
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Prior liver transplantation.
  • patients with concurrent malignancies other than HCC.

Other illness

  • Active autoimmune disease requiring systemic immunosuppression.

Other

  • Child-Pugh C liver function.

Who the study is looking for

  • 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) .

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
sSohag oncology centre
Coordinator of this site? Confirm its status
SohagEgyptUnknown status
Sohag university hospitals
Coordinator of this site? Confirm its status
SohagEgyptUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.