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Clinical Trial Summary

A randomised, cross-over study to compare quality of life and satisfaction in primary immunodeficient patients treated with subcutaneous injections of Gammanorm® 165 mg/mL administered with two different delivery devices: injections using pump or rapid push.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02503293
Study type Interventional
Source Octapharma
Contact
Status Completed
Phase Phase 4
Start date July 29, 2015
Completion date December 11, 2017

See also
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