A Study to Evaluate the Clinical Efficacy and Safety of Subcutaneously Administered C1-esterase Inhibitor in the Prevention of Hereditary Angioedema
A Double-blind, Randomized, Placebo-controlled, Cross-over Study to Evaluate the Clinical Efficacy and Safety of Subcutaneous Administration of Human Plasma-derived C1-esterase Inhibitor in the Prophylactic Treatment of Hereditary Angioedema
Sponsor: CSL Behring
A PHASE3 clinical study on Hereditary Angioedema Types I and II, this trial is completed. The trial is conducted by CSL Behring and has accumulated 11 data snapshots since 2014. Longitudinal tracking of this trial contributes to a broader understanding of treatment development timelines.
Status Flow
Change History
11 versions recorded-
Sep 2025 — Present [monthly]
Completed PHASE3
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Sep 2024 — Sep 2025 [monthly]
Completed PHASE3
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Jul 2024 — Sep 2024 [monthly]
Completed PHASE3
-
Feb 2021 — Jul 2024 [monthly]
Completed PHASE3
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Jan 2021 — Feb 2021 [monthly]
Completed PHASE3
▶ Show 6 earlier versions
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Jun 2018 — Jan 2021 [monthly]
Completed PHASE3
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Sep 2017 — Jun 2018 [monthly]
Completed PHASE3
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Jul 2017 — Sep 2017 [monthly]
Completed PHASE3
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May 2017 — Jul 2017 [monthly]
Completed PHASE3
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Feb 2017 — May 2017 [monthly]
Completed PHASE3
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Jan 2017 — Feb 2017 [monthly]
Completed PHASE3
First recorded
Jan 2014
Trial started
Per CT.gov start date — pre-dates our first snapshot
Eligibility Summary
No eligibility information available.
Contact Information
- CSL Behring
For direct contact, visit the study record on ClinicalTrials.gov .