CompletedPHASE1, PHASE2NCT01576523
A Study to Evaluate the Clinical Pharmacology and Safety of C1-esterase Inhibitor Administered by the Subcutaneous Route
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
- C1-esterase inhibitor - single intravenous dose(biological)
- Enrollment
- 18 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2012 – 2012
Study locations (8)
- Study Site, Atlanta, Georgia, United States
- Study Site, Chevy Chase, Maryland, United States
- Study Site, Cincinnati, Ohio, United States
- Study Site, Toledo, Ohio, United States
- Study Site, Hershey, Pennsylvania, United States
- Study Site, Berlin, Germany
- Study Site, Frankfurt, Germany
- Study Site, Mainz, Germany
Collaborators
Parexel
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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