drugset / Trial / NCT06903273

Neoadjuvant Tislelizumab, Gemcitabine, Cisplatin and S-1 for Resectable High-risk Cholangiocarcinoma

NCT06903273 ↗

NaSingle-groupOpen-labelTreatment

Summary

To investigate the efficacy and tolerability of neoadjuvant tislelizumab, gemcitabine, cisplatin and S-1 (TisGCS) in patients with resectable high-risk iCCA.

Timeline

Start
2025-07-01
Primary completion
2028-07-01
Completion
2029-07-01

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Cisplatin Other / unclassified 25 mg/m2 Intravenous
Subject Gemcitabine Small molecule 800 mg/m2 Intravenous
Subject S-1 Small molecule 35 mg/m2 Oral
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous

Indications