drugset / Trial / NCT00322556

Safety and Efficacy of Intravenous Immunoglobulin IgPro10 in Patients With Primary Immunodeficiencies (PID)

NCT00322556

Phase 3 Completed 55 enrolled CSL Behring
NaSingle-groupOpen-labelTreatment

Summary

The objectives of this trial are the assessment of safety and efficacy of IgPro10 in patients with PID, and the assessment of tolerability of high infusion rates. To demonstrate safety, the number of infusions temporally associated with AEs, the rate, severity and relationship of all AEs and the vital sign changes during each infusion will be evaluated.

Timeline

Start
2005-11
Primary completion
2008-04
Completion
2008-04

Drugs

EvaluationDrugModalityDoseRoute
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic 0.2 g/kg Intravenous
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic 0.8 g/kg Intravenous