CompletedPHASE1, PHASE2NCT01576523

A Study to Evaluate the Clinical Pharmacology and Safety of C1-esterase Inhibitor Administered by the Subcutaneous Route

Studying Hereditary angioedema

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Key facts

Sponsor
CSL Behring
Principal Investigator
Global Clinical Program Director
CSL Behring
Intervention
C1-esterase inhibitor - single intravenous dose(biological)
Enrollment
18 enrolled
Eligibility
18 years · All sexes
Timeline
20122012

Study locations (8)

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.

Open NCT01576523 on ClinicalTrials.gov

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