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OncoMatch/Clinical Trials/NCT06492408

Neoadjuvant Intra-tumor Double Immunotherapy for Hepatocellular Carcinoma.

Is NCT06492408 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies ipilimumab, pembrolizumab, durvalumab, idarubicin, bevacizumab for hepatic cancer.

Phase 2RecruitingSecond Affiliated Hospital of Guangzhou Medical UniversityNCT06492408Data as of Jun 2026Location: China

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

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Extracted eligibility criteria

Treatments studied

Immunotherapy

ipilimumab, pembrolizumab, durvalumab, idarubicin, bevacizumab

Performance status

ECOG 0–1(Restricted strenuous activity)

Demographics

Ages ≤ 75

Prior therapy

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

Cannot have received: clinical trial therapy

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

Cannot have received: any prior malignancy

Patients accompanied with other tumors or past medical history of malignancy

Lab requirements

Blood counts

ANC >= 1.5 x 10^9/L; Hemoglobin >= 8.0 g/dL; Platelets >= 100 x 10^9/L

Kidney function

Creatinine <= 1.5 x ULN or calculated creatinine clearance >= 50 mL/min using Cockcroft-Gault formula OR 24-hour urine creatinine clearance >= 50 mL/min

Liver function

Total bilirubin <= 1.5 x ULN (except subjects with Gilbert syndrome who can have total bilirubin < 3.0 mg/dL)

Absolute neutrophil count (ANC) >= 1.5 x 10^9/L; Hemoglobin >= 8.0 g/dL; Platelets >= 100 x 10^9/L; Total bilirubin <= 1.5 x upper limit of normal (ULN) (except subjects with Gilbert syndrome who can have total bilirubin < 3.0 mg/dL); Creatinine <= 1.5 x ULN or calculated creatinine clearance >= 50 mL/min using Cockcroft-Gault formula for creatinine clearance calculation OR 24-hour urine creatinine clearance >= 50 mL/min.

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

Frequently asked questions

Is NCT06492408 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.

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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