drugset / Trial / NCT05414032

Molecular Residual Disease Interception in Locoregionally-Advanced High Risk HPV+ and HPV- HNSCC

NCT05414032

RandomizedParallel-groupOpen-labelTreatment

Summary

This is a phase II, open-label study to assess the efficacy of AZD2936 in terms of molecular residual disease (MRD) clearance and treatment outcome in patients with MRD after definitive treatment for high risk locoregionally advanced head and neck squamous cell carcinoma (LA-HNSCC). MRD is defined as ctDNA detection in plasma after definitive treatment. Approximately 100 patients are expected to be enrolled.

Timeline

Start
2023-07-12
Primary completion
2027-09
Completion
2028-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Rilvegostomig Other / unclassified 750 mg Intravenous