drugset / Trial / NCT04620200

Neo-adjuvant Nivolumab or Nivolumab With Ipilimumab in Advanced Cutaneous Squamous Cell Carcinoma Prior to Surgery

NCT04620200 ↗

Phase 2 Completed 50 enrolled The Netherlands Cancer Institute
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

EvaluationDrugModalityDoseRoute
Subject Ipilimumab Monoclonal antibody 1 mg/kg —
Subject Nivolumab Monoclonal antibody 3 mg/kg —