drugset / Trial / NCT05001737

Evaluate Efficacy, Safety and Tolerability, PK and PD of Emapalumab in Children and Adults With MAS in Still's or SLE

NCT05001737

Phase 3 Completed 33 enrolled Swedish Orphan Biovitrum
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, tolerability and efficacy of emapalumab in children and adults with macrophage activation syndrome (sHLH/MAS) in Still's disease (including systemic juvenile idiopathic arthritis and adult onset Still's disease) or with sHLH/MAS in systemic lupus erythematous, resenting an inadequate response to high dose glucocorticoid treatment.

Timeline

Start
2021-12-15
Primary completion
2024-06-30
Completion
2025-06-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Emapalumab Monoclonal antibody Intravenous