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NCT05751343RecruitingPhase 2

Atezolizumab and Bevacizumab Plus TACE-HAIC for Unresectable Advanced HCC: a Phase 2 Clinical Trial

Atezolizumab Plus Bevacizumab Plus Transarterial Chemoembolization and Hepatic Artery Infusion Chemotherapy for Unresectable Advanced Hepatocellular Carcinoma: a Single-arm Phase 2 Clinical Trial

Source: ClinicalTrials.gov · Last updated 18 Nov 2025

Brief summary (registry, in English)

Atezolizumab and bevacizumab was approve for advanced unresectable hepatocellular carcinoma (aHCC). Whether the additional of transartial chemobolization and hepatic artery infusion chemotherapy will improve the response rate for those patients is still unknown. This phase 2 clinical trial aims to investigate the objective response rate for unresectable advanced hepatocellular carcinoma.

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
55 (estimated)
First submitted
20 Feb 2023
Start date
9 Mar 2023
Primary completion date
28 Aug 2024
Lead sponsor
Sun Yat-sen University
NCT number
NCT05751343

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 55
  • From 9 Mar 2023 to the primary completion date, 28 Aug 2024
  • 1 site 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

  • (c) contraindication to either atezolizumab and bevacizumab.

Other illness

  • (a) severe underlying cardiac, pulmonary, or renal diseases;
  • (b) history of a second primary malignant tumor;

Who the study is looking for

  • (a) patients were diagnozied with unresectable advanced-stage HCC,
  • (b) Child-Pugh A or B liver function;
  • (d) Eastern Cooperative Oncology Group (ECOG) performance status 0-1;
  • (e) adequate hematologic blood counts (white blood cell count \>3ⅹ109/L, absolute neutrophil count \>1.5ⅹ109/L, platelet count \>10ⅹ109/L, hemoglobin concentration \>85 g/L);

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

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

SiteCityCountrySite status
Sun Yat-sen University Cancer Center
Coordinator of this site? Confirm its status
GuangzhouChinaRecruiting

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