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Study identifier: NCT05613478 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Camrelizumab Combined With Apatinib Mesylate and TACE in the Perioperative Treatment of Hepatocellular Carcinoma

Condition: Hepatocellular Carcinoma · Immunotherapy · Preoperative  ·  Sponsor: The First Affiliated Hospital with Nanjing Medical University

PhasePhase 3
Planned participants130
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

Hepatocellular carcinoma (HCC) is the most common primary liver cancer. Hepatectomy is a curable and effective method. However, the recurrence rate is as high as 50%\~70% in 5 years after surgery. Perioperative treatment with immunotherapy combined with target therapy is expected to improve the patient's prognosis. This study aims to evaluate the efficacy, safety and tolerability of camrelizumab combined with apatinib mesylate in the perioperative period of resectable hepatocellular carcinoma. The primary purpose of this study is to evaluate 2 year event-free survival(2y-EFS) of camrelizumab combined with apatinib mesylate in the perioperative period of hepatocellular carcinoma (CNLC Ib-IIIa). The secondary research purpose is to evaluate the R0 resection rate, the rate of subjects with major pathological response, the rate of subjects with pathological complete response, event-free survival (EFS) and overall survival of camrelizumab combined with apatinib mesylate in the perioperative period of resectable hepatocellular carcinoma. The safety and tolerability is also evaluated.

This description comes directly from the study's public registry record.

Talk to the study team

Xuehao Wang, professor  ·  86-025-68303211  ·  Wangxh@njmu.edu.cn

Always discuss trial participation with your own doctor first.

Locations (1)

Jiangsu Province HospitalNanjing, Jiangsu, ChinaRecruiting

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Source record: clinicaltrials.gov/study/NCT05613478