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OncoMatch/Clinical Trials/NCT03949231

Infusion of PD1/PDL1/CTLA4 Inhibitors Via Hepatic Arterial for Immunotherapy of Hepatocellular Carcinoma

Is NCT03949231 recruiting? Yes, currently enrolling (Jun 2026). This Phase 3 trial studies PD1/PDL1 inhibitor for liver cancer.

Phase 3RecruitingSecond Affiliated Hospital of Guangzhou Medical UniversityNCT03949231Data as of Jun 2026Location: China

Treatment: PD1/PDL1 inhibitorThis trial was designed to investigate the survival outcomes, response rates, and safety of patients with Barcelona-Clinical Hepatocellular Carcinoma (BCLC)-C-stage liver cancer by hepatic artery versus vein infusion of PD1/PDL1/CTLA4 inhibitor or their combinations.

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Extracted eligibility criteria

Treatments studied

Other

PD1/PDL1 inhibitor

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 80

Prior therapy

Cannot have received: transplantation

Patients have the past history of liver cancer treatment, such as transplantation, resection, radiotherapy, chemotherapy and so on

Cannot have received: resection

Patients have the past history of liver cancer treatment, such as transplantation, resection, radiotherapy, chemotherapy and so on

Cannot have received: radiotherapy

Patients have the past history of liver cancer treatment, such as transplantation, resection, radiotherapy, chemotherapy and so on

Cannot have received: chemotherapy

Patients have the past history of liver cancer treatment, such as transplantation, resection, radiotherapy, chemotherapy and so on

Lab requirements

Blood counts

WBC ≥ 3.0×10E9/L; Hb ≥ 90g/L; PLT ≥ 50×10E9/L; INR < 2.3 or PT < 6 seconds above control

Kidney function

Cr ≤ 145.5 umul/L; Renal failure / insufficiency requiring hemo- or peritoneal dialysis [excluded]

Liver function

Child-Pugh class A or B/Child score > 7; Albumin > 28 g/L; Total bilirubin < 51 μmol/L

Child-Pugh class A or B/Child score > 7; WBC≥3.0×10E9/L; Hb≥90g/L; PLT ≥50×10E9/L;INR < 2.3 or PT < 6 seconds above control;Cr ≤ 145.5 umul/L;Albumin > 28 g/L;Total bilirubin < 51 μmol/L; Impaired clotting test (platelet count < 60000/mm3, prothrombin activity < 50%) [excluded]; Renal failure / insufficiency requiring hemo-or peritoneal dialysis [excluded]

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

Frequently asked questions

Is NCT03949231 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior transplantation, resection, radiotherapy disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 80 years or younger.

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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