drugset / Trial / NCT06680115

Neoadjuvant and Adjuvant Sintilimab Combined with Chemoradiotherapy Versus Chemoradiotherapy Alone in Stage TanyN3M0 Nasopharyngeal Carcinoma

NCT06680115 ↗

Phase 2 Not yet recruiting 150 enrolled First Affiliated Hospital of Guangxi Medical University
RandomizedParallel-groupOpen-labelTreatment

Summary

To evaluate the efficacy and safety of neoadjuvant and adjuvant Sintilimab combined with chemoradiotherapy versus chemoradiotherapy alone in stage TanyN3M0 nasopharyngeal carcinoma. The primary endpoint was 2-year failure-free survival (FFS). Secondary endpoints included 2-year overall survival (OS), distant failure-free survival (DFFS), locoregional failure-free survival (LRFFS), and adverse events.

Timeline

Start
2024-11
Primary completion
2026-12
Completion
2029-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Sintilimab Monoclonal antibody — —