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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


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

See also
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