drugset / Trial / NCT03838263

Feasibility and Tolerance of Nivolumab Neoadjuvant Immunotherapy in High Risk HPV Driven Oropharynx Cancer

NCT03838263 ↗

Phase 2 Completed 62 enrolled UNICANCER
RandomizedParallel-groupOpen-labelTreatment

Summary

The aim of this research is to study the feasibility of neoadjuvant treatment before chemoradiation in "high risk" HPV-driven Oropharynx cancer

Timeline

Start
2019-07-25
Primary completion
2022-04-01
Completion
2024-11-20

Outcome

Missed primary endpoint

paper The primary end point was not met: four of 41 patients in EA received <200 mg/m2 cisplatin. PMID 41570275 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Nivolumab Monoclonal antibody 240 mg Intravenous

Indications