drugset / Trial / NCT05744063

A Post-authorization Study to Describe the Safety and Efficacy of Emapalumab for the Treatment of pHLH in Treatment Experienced Chinese Patients

NCT05744063

Phase 4 Completed 13 enrolled Swedish Orphan Biovitrum
NaSingle-groupOpen-labelTreatment

Summary

The goal of this post-authorization study is to describe safety and efficacy of emapalumab in treatment experienced Chinese patients with pHLH.

Timeline

Start
2023-02-03
Primary completion
2025-02-21
Completion
2025-08-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Emapalumab Monoclonal antibody 1 mg/kg