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A European Multi-Center, Multi-Country, Post-Authorisation, Observational Study (Registry) Of Patients With Hereditary Angioedema (HAE) Who Are Administered CINRYZE® (C1 Inhibitor [Human]) For The Treatment Or Prevention Of HAE Attacks
This observational (non-interventional) study is being conducted to characterize the safety and use of CINRYZE in routine clinical practice when administered for (1) routine prevention of angioedema attacks, (2) pre-procedure prevention of angioedema attacks, and/or (3) treatment of angioedema attacks.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Universitair Ziekenhuis Antwerpen (UZA)
Antwerp, Edegem, Belgium
Clinic St-Luc University Hospital
Brussels, Belgium
CHU d'Angers
Angers, France
Hôpital Claude-Huriez
Lille, France
Immunologie Clinique et Allergologie
Nancy, France
Hôpital Saint Antoine
Paris, France
Université Paris Descartes
Paris, France
Allergie-Centrum-Charite
Berlin, Germany
Universitätsklinik Essen
Essen, Germany
Johann Wolfgang Goethe Universität
Frankfurt, Germany
Start Date
May 11, 2012
Primary Completion Date
September 25, 2016
Completion Date
September 25, 2016
Last Updated
March 17, 2021
83
ACTUAL participants
Lead Sponsor
Shire
NCT07298447
NCT06842823
NCT05469789
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
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