This is a phase 3, randomized, double-blind, placebo-controlled study to compare the efficacy and safety of tislelizumab (BGB-A317) versus placebo in combination with chemoradiotherapy in participants with localized esophageal squamous cell carcinoma (ESCC).
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Progression-free Survival (PFS)
Timeframe: From randomization to the prespecified primary analysis data cut-off date of 08 January 2025; maximum time on study was 67 months.