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Clinical Trial Summary

The investigators design a phase II clinical study to explore the efficacy and safety of Transarterial Chemoembolization (TACE) + Lenvatinib + Icaritin soft capsules in patients with Unresectable, non-metastatic hepatocellular carcinoma and to analyze potential biomarkers of therapeutic response.


Clinical Trial Description

This is a single-center, open-label, prospective, non-randomized clinical trial. We adopted the prospective cohort study to explore the safety and efficacy of Transarterial Chemoembolization (TACE) + Lenvatinib + Icaritin soft capsules in the patients with Unresectable, non-metastatic hepatocellular carcinoma. It is estimated that 20 patients who met the study criteria will be enrolled in Zhejiang Cancer Hospital. The investigators will follow up and collect subjects' data monthly to evaluate the efficacy and safety of treatment, including overall survival and time to progression. Multi-omics data analysis will be used to find potential biomarkers of treatment response. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05903456
Study type Interventional
Source Zhejiang Cancer Hospital
Contact guoliang Shao, doctor
Phone 13958183472
Email shaogl@zjcc.org.cn
Status Not yet recruiting
Phase Phase 2
Start date July 2023
Completion date December 2025

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