drugset / Trial / NCT01458171

Follow-up Study of Subcutaneous Immune Globulin in Patients Requiring IgG Replacement Therapy (Japan Study)

NCT01458171

Phase 3 Completed 23 enrolled CSL Behring
NaSingle-groupOpen-labelTreatment

Summary

The objective of this study is to assess the long-term safety, tolerability, and efficacy of IgPro20 in subjects with primary immunodeficiency (PID) as a follow-up to the pivotal study ZLB06\_002CR (NCT01199705).

Timeline

Start
2011-04
Primary completion
2012-02
Completion
2012-04

Drugs

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