drugset / Trial / NCT00546871

Comparison of Intravenous and Subcutaneous Administration of IGIV, 10% in Primary Immunodeficiency (PID) Subjects

NCT00546871

Phase 2/3 Completed 49 enrolled Baxalta now part of Shire
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the tolerability of IGIV, 10% given subcutaneously and the pharmacokinetics of immunoglobulin G (IgG) following subcutaneous (SC) treatment with IGIV, 10% in subjects with primary immunodeficiency (PID) disorders.

Timeline

Start
2007-10-03
Primary completion
2009-07-01
Completion
2009-09-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Immune Globulin Intravenous (Human) Protein / enzyme biologic Intravenous