CompletedNCT01108848
Patient Registry Study of Berinert® in Normal Clinical Practice
Studying Hereditary angioedema
Last synced from ClinicalTrials.gov
ℹ
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
- Berinert® (C1 Esterase Inhibitor)(biological)
- Enrollment
- 318 enrolled
- Eligibility
- All sexes
- Timeline
- 2010 – 2014
Study locations (30)
- United States, Arizona, Scottsdale, Arizona, United States
- United States, California, Granada Hills, California, United States
- United States, California, Los Angeles, California, United States
- United States, California, Redding, California, United States
- United States, California, San Diego, California, United States
- United States, Georgia, Atlanta, Georgia, United States
- United States, Idaho, Idaho Falls, Idaho, United States
- United States, Louisiana, New Orleans, Louisiana, United States
- United States, Maryland, Chevy Chase, Maryland, United States
- United States, Maryland, Columbia, Maryland, United States
- United States, Massachusetts, Boston, Massachusetts, United States
- United States, Minnesota, Plymouth, Minnesota, United States
- United States, Missouri, Kansas City, Missouri, United States
- United States, Missouri, St Louis, Missouri, United States
- United States, New Jersey, Branchburg, New Jersey, United States
- +15 more locations on ClinicalTrials.gov
Collaborators
Chiltern International Inc.
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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