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Recruiting Phase 2 NCT06406634

Cadonilimab in Combination With Lenvatinib and Hepatic Arterial Infusion Chemotherapy (HAIC) for the Treatment of Unresectable Hepatocellular Carcinoma

Trial Parameters

Condition Hepatocellular Carcinoma
Sponsor Hunan Cancer Hospital
Study Type INTERVENTIONAL
Phase Phase 2
Enrollment 30
Sex ALL
Min Age 18 Years
Max Age 75 Years
Start Date 2024-05-15
Completion 2026-04-20
Interventions
CadonilimabLenvatinib

Brief Summary

This study is an open-label, multicenter, single-arm Phase II clinical study to evaluate the effectiveness of Cadonilimab(AK104) in Combination With Lenvatinib and Hepatic Arterial Infusion Chemotherapy (HAIC) for the Treatment of Unresectable Hepatocellular Carcinoma

Eligibility Criteria

Inclusion Criteria: 1. The written informed consent form should be signed before a subject participates in the trial; 2. Histologically/cytologically confirmed HCC or cirrhosis meeting the clinical diagnostic criteria of HCC by the American Association for the Study of Liver Diseases (AASLD); 3. According to the Chinese Guidelines for Diagnosis and Treatment of Primary Liver Cancer (2022 edition), eligible for China liver cancer staging (CNLC) Stage IIIa and is not suitable for radical treatment, such as resection, ablation, or liver transplantation. Suitable for HAIC surgery and chemotherapy drugs prescribed in advance by the research center, without any contraindications to HAIC surgery and chemotherapy drugs; 4. Child-Pugh A or B; 5. at least 1 measurable lesion according to RECIST v1.1; 6. Eastern Cooperative Oncology Group performance status (ECOG PS) score of 0 or 1; 7. Adequate organ and marrow function, as defined below; 1) Absolute neutrophil count (ANC) ≥1.5x109/L without gra

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