drugset / Trial / NCT04308174

Neoadjuvant Gemcitabine Plus Cisplatin With or Without Durvalumab in Resectable Biliary Tract Cancer

NCT04308174 ↗

Phase 2 Active not recruiting 45 enrolled Asan Medical Center Samsung Medical Center · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

Considering that the poor prognosis of resected biliary tract cancer and negative impact on the survival outcomes of R1/R2 resection, neoadjuvant chemotherapy may improve R0 resection rates and the survival outcomes of patients with resectable biliary tract cancer. The addition of durvalumab to gemcitabine/cisplatin as neoadjuvant chemotherapy may improve the R0 resection rates compared to gemcitabine/cisplatin in patients with localized biliary tract cancer. In this phase 2 trial, a total of 45 patients with localized biliary tract cancer will be 2:1 randomized to durvalumab plus gemcitabine/cisplatin or gemcitabine/cisplatin.

Timeline

Start
2020-05-20
Primary completion
2023-06-30
Completion
2025-12-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Durvalumab Monoclonal antibody 1500 mg Intravenous
Comparator Cisplatin Other / unclassified 25 mg Intravenous
Comparator Gemcitabine Small molecule 1000 mg Intravenous