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OncoMatch/Clinical Trials/NCT06789757

The Study of Atezolizumab, Bevacizumab and Memantine in Patients With Hepatocellular Carcinoma (HCC)

Is NCT06789757 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies multiple treatments including Memantine Hydrochloride and Bevacizumab for hepatocellular carcinoma.

Phase 2RecruitingInova Health Care ServicesNCT06789757Data as of May 2026

Treatment: Memantine Hydrochloride · Bevacizumab · AtezolizumabThe purpose of this research is to see the effect of triplet therapy with atezolizumab, bevacizumab, and memantine in treatment of your hepatocellular carcinoma.

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

No prior treatment (treatment-naive required)

Cannot have received: memantine (memantine)

Patients already on memantine for any reason prior to enrollment will be excluded

Lab requirements

Blood counts

Absolute Neutrophil Count ≥ 1,500/μL; Platelets ≥ 100,000/μL; Hemoglobin ≥ 90 g/L (9g/dL)

Kidney function

Creatinine ≤ 2.0 mg/dL; eGFR (using Cockcroft Gault equation) > 40ml/min

Liver function

Childs-Pugh cirrhosis score of A5 or A6; Total Bilirubin ≤ 3 x ULN; AST(SGOT)/ALT(SGPT)/Alkaline Phosphatase ≤ 3 x ULN Or ≤5x ULN if due to liver involvement by tumor

Cardiac function

No significant cardiovascular disease (such as NYHA Class II or greater cardiac disease, myocardial infarction, or cerebrovascular accident) within 3 months prior to initiation of study treatment, unstable arrhythmia, or unstable angina

Patients must have bone marrow and organ function as defined below: Absolute Neutrophil Count ≥ 1,500/μL; Platelets ≥ 100,000/μL; Hemoglobin ≥ 90 g/L (9g/dL); Total Bilirubin ≤ 3 x ULN; AST(SGOT)/ALT(SGPT)/Alkaline Phosphatase ≤ 3 x ULN Or ≤5x ULN if due to liver involvement by tumor; Creatinine ≤ 2.0 mg/dL; eGFR (using Cockcroft Gault equation) > 40ml/min. Significant cardiovascular disease (such as New York Heart Association Class II or greater cardiac disease, myocardial infarction, or cerebrovascular accident) within 3 months prior to initiation of study treatment, unstable arrhythmia, or unstable angina [excluded].

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

US trial sites

  • Inova Schar Cancer Institute - Fair Oaks · Fairfax, Virginia
  • Inova Health Care Service · Falls Church, Virginia

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

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