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OncoMatch/Clinical Trials/NCT06482801

Checkpoint Inhibitor Combinations Therapy as First Line for HCC Via IT

Is NCT06482801 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies ipilimumab+pembrolizumab or ipilimumab+durvalumab, idarubicin, bevacizumab for liver cancer.

Phase 2RecruitingSecond Affiliated Hospital of Guangzhou Medical UniversityNCT06482801Data as of Jun 2026Location: China

Treatment: ipilimumab+pembrolizumab or ipilimumab+durvalumab, idarubicin, bevacizumabThis trial is designed to investigate the safety, response rates and survival outcomes of patients with hepatocellular carcinoma by infusion of CTLA4, PD1 and PDL1 antibodies combination with chemodrug or/and bevacizumab through intra-tumor (IT).

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Extracted eligibility criteria

Treatments studied

Immunotherapy

ipilimumab+pembrolizumab or ipilimumab+durvalumab, idarubicin, bevacizumab

Cancer type

Hepatocellular Carcinoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

Cannot have received: clinical trial agent or device

Patients participated in clinical trials of equipment or drugs (signed informed consent) within 4 weeks

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; Impaired clotting test (platelet count < 60000/mm3, prothrombin activity < 50%) [excluded]

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 NCT06482801 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior clinical trial agent or device disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 75 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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