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Clinical Trial Summary

The purpose of the study is to determine the feasibility of infusing a full 4-week dose of Immune Globulin Intravenous (Human), 10% in a single subcutaneous site and the amount of recombinant human hyaluronidase needed to infuse that dose with no more than mild local adverse drug reactions.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00782106
Study type Interventional
Source Takeda
Contact
Status Completed
Phase Phase 1/Phase 2
Start date December 4, 2006
Completion date November 1, 2007

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