WithdrawnPhase 2NCT01832896

Study to Assess the Tolerability and Safety of Ecallantide in Children and Adolescents With Hereditary Angioedema

Studying Hereditary angioedema

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Key facts

Sponsor
NYU Langone Health
Principal Investigator
Mark A Davis-Lorton, MD
Winthrop University Hospital
Intervention
Ecallantide subcutaneous dosing(drug)
Eligibility
2-16 years · All sexes
Timeline
20132017

Study locations (1)

Collaborators

Dyax Corp.

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 NCT01832896 on ClinicalTrials.gov

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