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Clinical Trial Summary

CLINICAL PHASE 3 STUDY TO MONITOR THE SAFETY, TOLERABILITY, AND EFFICACY OF SUBCUTANEOUS HUMAN IMMUNOGLOBULIN (CUTAQUIG®) ADMINISTERED AT MODIFIED DOSING REGIMENS IN PATIENTS WITH PRIMARY IMMUNODEFICIENCY DISEASES


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03939533
Study type Interventional
Source Octapharma
Contact
Status Completed
Phase Phase 3
Start date October 17, 2019
Completion date January 3, 2022

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