drugset / Trial / NCT07100392

Tauroursodeoxycholic Acid (TUDCA) Plus Camrelizumab and Regorafenib in Hepatocellular Carcinoma Previously Treated With Anti-PD1/PD-L1 and Bevacizumab

NCT07100392

Phase 2 Recruiting 141 enrolled Fudan University
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the efficacy and safety of Tauroursodeoxycholic Acid (TUDCA) plus Camrelizumab and Regorafenib for patients with advanced hepatocellular carcinoma (HCC) who have progressed on prior systemic treatment with Anti-PD1/PD-L1 plus bevacizumab combination.

Timeline

Start
2025-08-14
Primary completion
2027-08-01
Completion
2028-08-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Camrelizumab Monoclonal antibody 200 mg Intravenous
Subject Regorafenib Small molecule 80 mg Oral
Subject Taurursodiol Small molecule 250 mg Oral