drugset / Trial / NCT06031233

Evaluating the Safety of Shortened Infusion Times for dIfferent Oncological Immunotherapie

NCT06031233 ↗

Phase 4 Recruiting 776 enrolled Isala
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This study is an interventional, explorative, prospective study to show whether shortening of infusion times for patients using nivolumab, pembrolizumab, ipilimumab, trastuzumab, bevacizumab, durvalumab or atezolizumab continues to be associated with an acceptable safety profile. Infusion times will be gradually shortened if tolerability allowes.

Timeline

Start
2023-09-01
Primary completion
2028-07
Completion
2028-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Atezolizumab Monoclonal antibody — —
Subject Bevacizumab Monoclonal antibody — —
Subject Durvalumab Monoclonal antibody — —
Subject Ipilimumab Monoclonal antibody — —
Subject Nivolumab Monoclonal antibody — —
Subject Pembrolizumab Monoclonal antibody — —
Subject Rituximab Monoclonal antibody — —
Subject Trastuzumab Monoclonal antibody — —

Indications

No indication recorded.