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OncoMatch/Clinical Trials/NCT06710223

Cryoablation and Arterial Infusion of SD-101 in Combination with Durvalumab and Tremelimumab

Is NCT06710223 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies multiple treatments including SD-101 and Cryotherapy for hepatocellular carcinoma.

Phase 1RecruitingUniversity of California, San DiegoNCT06710223Data as of Jun 2026

Treatment: SD-101 · Cryotherapy · Tremelimumab · DurvalumabThe goal of this Phase 1b clinical trial is to evaluate the safety and efficacy of cryoablation and hepatic arterial administration of SD-101 in participants with advanced hepatocellular carcinoma. After this procedure, participants will be treated with tremelimumab and durvalumab every 4 weeks (STRIDE regimen).

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Extracted eligibility criteria

Treatments studied

Immunotherapy

TremelimumabDurvalumab

Other

SD-101Cryotherapy

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

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

Lab requirements

Blood counts

Peripheral absolute neutrophil count ≥ 1000/mm^3; Platelet count ≥ 50,000/ mm^3; Hemoglobin ≥ 8.0 g/dL

Kidney function

creatinine clearance ≥ 50 ml/min

Liver function

Child-Pugh A or Child-Pugh B7 liver function; Total bilirubin ≤ 2.0 x institution's upper limit of normal; ALT or AST ≤ 5 x institution's upper limit of normal; Albumin ≥ 2 g/dL

Cardiac function

Systolic blood pressure <160 mm Hg; no NYHA class III/IV heart failure; no myocardial infarction/active ischemic heart disease within one year; no uncontrolled dysrhythmias; no poorly controlled angina

Child-Pugh A or Child-Pugh B7 liver function. Total bilirubin ≤ 2.0 x institution's upper limit of normal. ALT or AST ≤ 5 x institution's upper limit of normal. Albumin ≥ 2 g/dL. Peripheral absolute neutrophil count ≥ 1000/mm^3. Platelet count ≥ 50,000/ mm^3. Hemoglobin ≥ 8.0 g/dL. Creatinine clearance ≥ 50 ml/min. Systolic blood pressure <160 mm Hg. Cardiac impairment defined as: prior history of cardiovascular disease including heart failure that meets New York Heart Association (NYHA) class III and IV definitions; OR history of myocardial infarction/active ischemic heart disease within one year of study entry; OR uncontrolled dysrhythmias; OR poorly controlled angina.

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

US trial sites

  • University of California, San Diego · San Diego, California

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Frequently asked questions

Is NCT06710223 currently recruiting?

Yes, this trial is currently recruiting patients.

Can patients have received prior systemic therapy?

No. This trial requires treatment-naive patients — prior systemic therapy is an exclusion criterion.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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