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Clinical Trial Summary

To learn if giving immune checkpoint therapy (such as atezolizumab) and bevacizumab to patients who have HCC and are receiving DAAs may help to control HCC and hepatitis C.


Clinical Trial Description

Primary Objective(s): - Estimate the objective response rate (ORR) to ICT and estimate the sustained virologic response (SVR) in patients with HCC and chronic HCV infection using HCV clearance with DAA therapy. - Estimate the change of the overall T cells and virus-specific T cells before and after the antiviral treatment in patients with HCC and chronic HCV infection using HCV clearance with DAA therapy. Secondary objective: --Collect the safety profile of the treatment and estimate the time-to-event variable such as overall survival (OS) and progression free survival (PFS). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05717400
Study type Interventional
Source M.D. Anderson Cancer Center
Contact Harrys A Torres, MD
Phone 713) 792-6503
Email htorres@mdanderson.org
Status Recruiting
Phase Phase 4
Start date February 7, 2023
Completion date October 31, 2026

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