CompletedPhase 3NCT01912456
A Study to Evaluate the Clinical Efficacy and Safety of Subcutaneously Administered C1-esterase Inhibitor in the Prevention of Hereditary Angioedema
Studying Hereditary angioedema
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CSL Behring
- Principal Investigator
- Global Clinical Program DirectorCSL Behring
- Intervention
- Low-volume C1-esterase inhibitor(biological)
- Enrollment
- 90 enrolled
- Eligibility
- 12 years · All sexes
- Timeline
- 2014 – 2015
Study locations (30)
- Study Site, Birmingham, Alabama, United States
- Study Site, Scottsdale, Arizona, United States
- Study Site, Bell Gardens, California, United States
- Study Site, La Jolla, California, United States
- Study Site, Orange, California, United States
- Study Site, Walnut Creek, California, United States
- Study Site, Colorado Springs, Colorado, United States
- Study Site, Chevy Chase, Maryland, United States
- Study Site, Boston, Massachusetts, United States
- Study Site, Cincinnati, Ohio, United States
- Study Site, Columbus, Ohio, United States
- Study Site, Toledo, Ohio, United States
- Study Site, Tulsa, Oklahoma, United States
- Study Site, Lake Oswego, Oregon, United States
- Study Site, Hershey, Pennsylvania, United States
- +15 more locations on ClinicalTrials.gov
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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