drugset / Trial / NCT05233358

HAIC Combined With Second-line "Target Immunity" for HCC With TACE Standard Treatment Low Response or Failure

NCT05233358

RandomizedParallel-groupDouble-blindTreatment

Summary

This study is a prospective, randomized controlled, multicenter clinical study. The purpose of this study is to explore the efficacy and safety of hepatic artery infusion chemotherapy (HAIC) combined with second-line regorafenib and immune checkpoint inhibitors in the treatment of transarterial chemoembolization (TACE) combined with first-line molecular targeted drugs and immune checkpoint inhibitors with low response or failure in advanced hepatocellular carcinoma.

Timeline

Start
2022-02-01
Primary completion
2023-02-01
Completion
2025-02-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Background Camrelizumab Monoclonal antibody 200 mg Intravenous
Background Nivolumab Monoclonal antibody 200 mg Intravenous
Background Pembrolizumab Monoclonal antibody 200 mg Intravenous
Background Regorafenib Small molecule 80 mg Oral
Background Regorafenib Small molecule 160 mg Oral
Background Sintilimab Monoclonal antibody 200 mg Intravenous
Background Toripalimab Monoclonal antibody 200 mg Intravenous