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Clinical Trial Summary

This study is a single-center, open, single-arm, phase II clinical trial. Eligible HCC patients, after signing informed consent, will receive TACE treatment. Envafolimab combined with Lenvatinib will be started on the day of TACE, and the subsequent TACE will be performed on demand. Patients will receive the treatment continuously until disease progression or intolerance. Tumor imaging evaluation will be performed according to RECIST V1.1 criteria every 6 weeks. Safety will be assessed with CTCAE 5.0. Adverse events throughout and within 30 days of the end of the study will be recorded (severe adverse events or adverse events associated with Envafolimab will be recorded within 90 days after the end of treatment).Treatment will last for 2 years or until disease progression, withdrawal of informed consent, loss of visit, or death.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05213221
Study type Interventional
Source Zhejiang University
Contact Tingbo Liang, PhD
Phone +86 19941463683
Email [email protected]
Status Recruiting
Phase Phase 2
Start date March 14, 2022
Completion date January 1, 2024

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