At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
A Phase 2, Multicenter, Open-label, 2-Cohort Study to Investigate the Efficacy and Safety of PET Guided Neoadjuvant Treatment With Tislelizumab (BGB-A317) Plus Chemotherapy/Chemoradiotherapy in Patients With Resectable Esophageal Squamous Cell Carcinoma
In Brief
A Phase 2 clinical trial evaluating Tislelizumab, Paclitaxel, and 4 other interventions for Resectable Esophageal Squamous Cell Carcinoma. Completed, enrolled 70 participants across 8 sites.
Detailed Summary
The purpose of this study is to evaluate the pathological complete response (pCR) in participants receiving tislelizumab plus chemotherapy/chemoradiotherapy as neoadjuvant treatment.
Study Details
Timeline
Interventions
Administered intravenously on Day 1 of each 21-Day Cycle.
135 mg/m\^2 administered intravenously on Day 1 of each 21-Day Cycle.
80 mg/m\^2 administered intravenously on Day 1 of each 21-Day Cycle.
1000 mg/m\^2 administered intravenously over Day 1 through 4 of each 21-Day Cycle.
40 grays/20 fractions
Performed as indicated in the treatment arm.