Hereditary Angioedema

Human C1 Esterase Inhibitor (C1-INH) in Subjects With Acute Abdominal or Facial Hereditary Angioedema (HAE) Attacks
NCT00168103 | PHASE 2 | INTERVENTIONAL

HAE is a rare disorder characterized by functional C1 esterase inhibitor deficiency. If not treated adequately, the acute attacks of HAE can be life-threatening and may even result in fatalities, especially in case of swelling of the larynx. This clinical Phase 2/Phase 3 study was designed to provide clinically relevant data on dosing, efficacy and safety in subjects with HAE.

Trial Information
36 Sites
126 Participants
Recruiting
6 Years to 8 Years

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SUBMIT
Study Site
Granada Hills,California,United States,91344
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Weston,Florida,United States,33331
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Atlanta,Georgia,United States,30342
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Idaho Falls,Idaho,United States,83404
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Chicago,Illinois,United States,60612
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Shreveport,Louisiana,United States,71130
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Boston,Massachusetts,United States,02115
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Plymouth,Minnesota,United States,55411
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Omaha,Nebraska,United States,68131
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Bronx,New York,United States,10461
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Cincinnati,Ohio,United States,45231
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Tulsa,Oklahoma,United States,74133
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Eugene,Oregon,United States,97401
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Hershey,Pennsylvania,United States,17033
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Rapid City,South Dakota,United States,57702
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Dallas,Texas,United States,75230
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Bellingham,Washington,United States,98225
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Buenos Aires,Argentina
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Westmead,Australia
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Plovdiv,Bulgaria
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Sofia,Bulgaria
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Edmonton,Canada
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Ottawa,Canada
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Brno,Czech Republic
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Budapest,Hungary
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Tel Hashomer,Israel
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Skopje,Macedonia, The Former Yugoslav Republic of
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Grodzisk Mazowiecki,Poland
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Krakow,Poland
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Tirgu-Mures,Romania
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Moscow,Russian Federation
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Moscow,Russian Federation
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Moscow,Russian Federation
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Madrid,Spain
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Goeteborg,Sweden
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London,United Kingdom

Study Eligibility Criteria

Additional Studies

Additional studies can be found at ClinicalTrials.gov