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An Open-label, Randomized Study to Evaluate the Long-term Clinical Safety and Efficacy of Subcutaneous Administration of Human Plasma-derived C1-esterase Inhibitor in the Prophylactic Treatment of Hereditary Angioedema
Conditions
Interventions
C1-esterase inhibitor
Locations
32
United States
Study Site
Birmingham, Alabama, United States
Study Site
Scottsdale, Arizona, United States
Study Site
La Jolla, California, United States
Study Site
Orange, California, United States
Study Site
Walnut Creek, California, United States
Study Site
Chevy Chase, Maryland, United States
Start Date
December 31, 2014
Primary Completion Date
September 21, 2017
Completion Date
September 21, 2017
Last Updated
November 14, 2018
Lead Sponsor
CSL Behring
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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