drugset / Trial / NCT07208526

Summary

This project aims to conduct a prospective, multicenter, randomized controlled clinical trial. The study plans to enroll 270 patients with locally advanced iCCA who have successfully undergone GOLP conversion therapy. Participants will be randomized at a 1:2:2 ratio into three arms: Control Arm (continued medication), Direct Surgery Arm, and TDTP-RECIST Assessment Arm. The primary endpoint is Overall Survival (OS).

Timeline

Start
2025-12-01
Primary completion
2028-06-30
Completion
2028-12-31

Publications

Drugs

EvaluationDrugModalityDoseRoute
Comparator Lenvatinib Small molecule
Comparator Toripalimab Monoclonal antibody