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Gammagard Liquid and rHuPH20 in PID

Primary Immunodeficiency Diseases (PID) Clinical Trial

Official title:
Efficacy, Tolerability and Pharmacokinetic Comparison of Immune Globulin Intravenous (Human), 10% (GAMMAGARD LIQUID/KIOVIG) Administered Intravenously or Subcutaneously Following Administration of Recombinant Human Hyaluronidase (rHuPH20) in Subjects With Primary Immunodeficiency Diseases

Clinical Trial Summary

The purpose of the study is to develop a subcutaneous treatment option for participants with Primary Immunodeficiency Diseases (PID) that allows an administration of Immune Globulin Intravenous (Human), 10% at the same frequency as IV administration.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00814320
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 3
Start date December 18, 2008
Completion date November 11, 2010
View Details
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