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OncoMatch/Clinical Trials/NCT05701488

SIRT With Tremelimumab and Durvalumab for Resectable HCC

Is NCT05701488 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including Durvalumab and Tremelimumab for resectable hepatocellular carcinoma.

Phase 1RecruitingJiping Wang, MD, PhDNCT05701488Data as of May 2026

Treatment: Durvalumab · Tremelimumab · SIRTThe goal of this research study is to evaluate the safety and tolerability of tremelimumab and durvalumab with or without Selective Internal Yttrium-90 Radioembolization (SIRT) in participants with resectable hepatocellular carcinoma (HCC) who will undergo liver surgery. The names of the interventions involved in this study are: * Durvalumab (a type of immunotherapy) * Tremelimumab (a type of immunotherapy) * Selective Internal Yttrium-90 Radioembolization (SIRT) (a type of radiation microsphere bead)

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Extracted eligibility criteria

Cancer type

Hepatocellular Carcinoma

Disease stage

Required: Stage IA, IB, II, IIIA

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Cannot have received: any prior treatment for hcc

Lab requirements

Blood counts

hemoglobin ≥ 9.0 g/dl; absolute neutrophil count (anc) ≥ 1,000 /mcl; platelets ≥ 80,000 /mcl

Kidney function

measured creatinine clearance > 40 ml/min by 24-hour urine collection, or calculated creatinine clearance (cl) > 40 ml/min by the cockcroft-gault formula

Liver function

total bilirubin ≤ 2.0 mg/dl; ast (sgot) and alt (sgpt) ≤ 2.5 × institutional upper limit of normal (uln); preserved liver function (child a)

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

US trial sites

  • Cedars-Sinai Medical Center · Los Angeles, California
  • Beth Israel Deaconess Medical Center · Boston, Massachusetts
  • Dana-Farber Cancer Institute · Boston, Massachusetts

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