drugset / Trial / NCT01581593

Efficacy and Safety Study of Kedrion IVIG 10% to Treat Subjects With Primary Immunodeficiency (PID)

NCT01581593 ↗

Phase 3 Completed 45 enrolled Kedrion S.p.A.
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether Kedrion IVIG 10% (an immunoglobulin solution) is effective in treating Primary Immunodeficiency (PID).

Timeline

Start
2012-11-12
Primary completion
2014-08-27
Completion
2014-08-27

Drugs

EvaluationDrugModalityDoseRoute
Subject Kedrion IVIG 10% Protein / enzyme biologic 300 mg/kg Intravenous
Subject Kedrion IVIG 10% Protein / enzyme biologic 900 mg/kg Intravenous

Indications