Safety and Tolerability of Higher Infusion Parameters of IgPro20 (Hizentra) in Subjects With Primary Immunodeficiency (PID)
An Open-label Multicenter Study to Evaluate the Safety and Tolerability of Higher Infusion Parameters of Immune Globulin Subcutaneous (Human), 20% Liquid (Hizentra®) in Subjects With Primary Immunodeficiency
Sponsor: CSL Behring
A PHASE4 clinical study on Primary Immunodeficiency, this trial is completed. The trial is conducted by CSL Behring and has accumulated 19 data snapshots since 2017. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
19 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE4
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE4
-
Jul 2024 — Sep 2024 [monthly]
Completed PHASE4
-
Mar 2022 — Jul 2024 [monthly]
Completed PHASE4
-
Jan 2022 — Mar 2022 [monthly]
Completed PHASE4
▶ Show 14 earlier versions
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Jan 2021 — Jan 2022 [monthly]
Completed PHASE4
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Apr 2020 — Jan 2021 [monthly]
Completed PHASE4
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Feb 2020 — Apr 2020 [monthly]
Completed PHASE4
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Feb 2019 — Feb 2020 [monthly]
Completed PHASE4
Status: Active Not Recruiting → Completed
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Jan 2019 — Feb 2019 [monthly]
Active Not Recruiting PHASE4
Status: Recruiting → Active Not Recruiting
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Dec 2018 — Jan 2019 [monthly]
Recruiting PHASE4
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Jul 2018 — Dec 2018 [monthly]
Recruiting PHASE4
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Jun 2018 — Jul 2018 [monthly]
Recruiting PHASE4
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Dec 2017 — Jun 2018 [monthly]
Recruiting PHASE4
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Sep 2017 — Dec 2017 [monthly]
Recruiting PHASE4
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Aug 2017 — Sep 2017 [monthly]
Recruiting PHASE4
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Jul 2017 — Aug 2017 [monthly]
Recruiting PHASE4
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Jun 2017 — Jul 2017 [monthly]
Recruiting PHASE4
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Feb 2017 — Jun 2017 [monthly]
Recruiting PHASE4
First recorded
Eligibility Summary
No eligibility information available.
Contact Information
- CSL Behring
For direct contact, visit the study record on ClinicalTrials.gov .