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Clinical Trial Summary

This is a single arm and open-label phase I trial to evaluate the safety, tolerability and efficacy of the oncolytic virus M1 (M1-c6v1)(iv 1×109 CCIC50, 1 dose per day, on day 1-5 each 28 day cycle) combined with anti-PD-1 antibody SHR-1201 (iv, 200 mg, once every two weeks) and Apatinib (po. 250 mg qd ) in the patients with advanced/metastatic hepatocellular carcinoma. 10 participants will be sequentially enrolled. The treatment duration is 12 months. All patients continue combination treatment until disease progression, unacceptable toxicity, death, or discontinuation for any reason.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04665362
Study type Interventional
Source Third Affiliated Hospital, Sun Yat-Sen University
Contact Liang Peng, MD
Phone 8613533978874
Email pliang@mail.sysu.edu.cn
Status Not yet recruiting
Phase Phase 1
Start date January 25, 2021
Completion date October 30, 2022