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Clinical Trial Summary

The purpose of this study is to investigate the efficacy, safety, tolerability, and pharmacokinetic profile of the investigational medicinal product (IMP) and to determine, on the basis of historical control data, how it compares with other 10% intravenous immunoglobulin (IGIV) products currently licensed in North America for the treatment of subjects with primary immune deficiency diseases (PIDD).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03238079
Study type Interventional
Source Therapure Biopharma Inc
Contact
Status Active, not recruiting
Phase Phase 3
Start date September 5, 2017
Completion date December 30, 2020