drugset / Trial / NCT03838263
Feasibility and Tolerance of Nivolumab Neoadjuvant Immunotherapy in High Risk HPV Driven Oropharynx Cancer
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Nivolumab | Monoclonal antibody | 240 mg | Intravenous |