drugset / Trial / NCT04974047

Study of Tislelizumab in Participants With Resectable Esophageal Squamous Cell Carcinoma

NCT04974047 ↗

Phase 2 Completed 70 enrolled BeiGene
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the pathological complete response (pCR) in participants receiving tislelizumab plus chemotherapy/chemoradiotherapy as neoadjuvant treatment.

Timeline

Start
2021-08-17
Primary completion
2023-04-17
Completion
2024-10-25

Drugs

EvaluationDrugModalityDoseRoute
Subject Paclitaxel Small molecule 135 mg/m2 Intravenous
Subject Tislelizumab Monoclonal antibody 200 mg Intravenous
Subject fluorouracil Small molecule 1000 mg/m2 Intravenous
Background Cisplatin Other / unclassified 80 mg/m2 Intravenous