drugset / Trial / NCT03961009

Clinical Assessment of Pharmacokinetics, Efficacy, and Safety of 10% IVIg in PID Patients

NCT03961009 ↗

Phase 3 Completed 47 enrolled Kedrion S.p.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to assess efficacy and safety of Kedrion Immunoglobulin 10% (KIg10) in participants with Primary Immunodeficiency (PID).

Timeline

Start
2019-04-30
Primary completion
2020-12-21
Completion
2020-12-21

Drugs

EvaluationDrugModalityDoseRoute
Subject KIg10 Protein / enzyme biologic 200 mg/kg Intravenous
Subject KIg10 Protein / enzyme biologic 800 mg/kg Intravenous