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OncoMatch/Clinical Trials/NCT06096779

A Study Evaluating Atezolizumab, With or Without Bevacizumab, in Participants With Unresectable Hepatocellular Carcinoma and Child-pugh B7 and B8 Cirrhosis

Is NCT06096779 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Atezolizumab and Bevacizumab for hepatocellular carcinoma.

Phase 2RecruitingGenentech, Inc.NCT06096779Data as of May 2026

Treatment: Atezolizumab · BevacizumabThe purpose of this study is to assess the safety of atezolizumab and bevacizumab, or atezolizumab alone, as first-line treatment in participants with unresectable, locally advanced or metastatic hepatocellular carcinoma (HCC) with Child-pugh B7 or B8 cirrhosis.

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: systemic therapy

No prior systemic treatment (including systemic investigational agents) for locally advanced or metastatic and/or unresectable HCC

Cannot have received: immune checkpoint blockade therapy

Prior treatment with cluster of differentiation 137 (CD137) agonists or immune checkpoint blockade therapies

Cannot have received: systemic immunostimulatory agent

Treatment with systemic immunostimulatory agents

Cannot have received: systemic immunosuppressive medication

Treatment with systemic immunosuppressive medication

Cannot have received: investigational therapy

Treatment with investigational therapy within 28 days prior to initiation of study treatment

Cannot have received: locoregional therapy to liver

Treatment with locoregional therapy to liver within 28 days prior to initiation of study treatment, or non-recovery from side effects of any such procedure

Lab requirements

Blood counts

Absolute neutrophil count ≥1.0 x 10^9 per liter (/L) (≥1000 per microliter [/μL]) without granulocyte colony-stimulating factor support; Platelet count ≥ 50 × 10^9/L (50,000/μL) without transfusion; Hemoglobin ≥ 80 grams per liter (g/L) (8 grams per deciliter [g/dL])

Kidney function

Creatinine clearance ≥ 50 milliliters per minute (mL/min) (calculated using the Cockcroft-gault formula)

Liver function

Child-pugh B7 or B8 cirrhosis at screening and within 7 days prior to study treatment; AST and ALT ≤ 5 × ULN; Serum bilirubin ≤ 3 × ULN; Serum albumin ≥ 20 g/L (2.0 g/dL) without transfusion in the prior 3 months; INR ≤2.3

Adequate hematologic and end-organ function Absolute neutrophil count ≥1.0 x 10^9 per liter (/L) (≥1000 per microliter [/μL]) without granulocyte colony-stimulating factor support Platelet count ≥ 50 × 10^9/L (50,000/μL) without transfusion Hemoglobin ≥ 80 grams per liter (g/L) (8 grams per deciliter [g/dL]) AST and ALT ≤ 5 × ULN Serum bilirubin ≤ 3 × ULN Creatinine clearance ≥ 50 milliliters per minute (mL/min) (calculated using the Cockcroft-gault formula) Serum albumin ≥ 20 g/L (2.0 g/dL) without transfusion in the prior 3 months International normalized ratio (INR) ≤2.3

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • University of Arizona Cancer Center · Tucson, Arizona
  • UC San Diego Moores Cancer Center · La Jolla, California
  • University of Southern California-Keck School of Medicine -1975 Zonal Ave · Los Angeles, California
  • University of Southern California · Newport Beach, California
  • University of California Irvine Medical Center · Orange, California

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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