drugset / Trial / NCT07152769

Iparomlimab and Tuvonralimab Combined With GC in Advanced ICC

NCT07152769

Phase 2 Not yet recruiting 104 enrolled Fudan University
RandomizedParallel-groupOpen-labelTreatment

Summary

This study is a randomized, controlled, open-label, single center clinical study. This study is designed to evaluate the efficacy and safety of Iparomlimab and Tuvonralimab Combined With GC versus Sintilimab Combined With GC as first-line therapy in advanced ICC.

Timeline

Start
2025-10-15
Primary completion
2028-02-29
Completion
2028-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject Iparomlimab Monoclonal antibody 5 mg/kg
Comparator Sintilimab Monoclonal antibody 5 mg/kg
Subject Tuvonralimab Monoclonal antibody 5 mg/kg
Comparator Cisplatin Other / unclassified 25 mg/m2
Comparator Gemcitabine Small molecule 1000 mg/m2