drugset / Trial / NCT04620200
Neo-adjuvant Nivolumab or Nivolumab With Ipilimumab in Advanced Cutaneous Squamous Cell Carcinoma Prior to Surgery
RandomizedParallel-groupOpen-labelTreatment
Summary
To determine the histopathological response rate to neo-adjuvant nivolumab and nivolumab plus ipilimumab at time of standard of care(surgery ± radiotherapy).in patients with cutaneous squamous cell carcinoma.
Timeline
- Start
- 2020-08-11
- Primary completion
- 2025-01-07
- Completion
- 2025-01-07
Outcome
Met primary endpoint
paper In the MATISSE trial, the primary objective was met to investigate the pathological response rate PMID 41062829 ↗
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Ipilimumab | Monoclonal antibody | 1 mg/kg | — |
| Subject | Nivolumab | Monoclonal antibody | 3 mg/kg | — |