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Retrospective, Observational Chart Review Study Evaluating Clinical Effectiveness and Disease/Treatment Management Among Patients Who Initiated Long-term Prophylaxis With Takhzyro® in a Real-world Setting
The main aims of this study are to learn how many people with HAE Type I or Type II are attack-free when treated with lanadelumab in real life. This includes the number of people that are attack-free when lanadelumab is given every 2 and every 4 weeks. This study is about collecting existing data only; participants will not receive lanadelumab as part of this study. No new information will be collected during this study. Only data already available at the participant's doctor's office will be reviewed and collected for this study. Participants do not need to visit their doctor in addition to their normal visits.
Age
12 - No limit years
Sex
ALL
Healthy Volunteers
No
LKH-Universitätsklinikum Klinikum Graz
Graz, Austria
Kepler Universitätsklinikum Linz
Linz, Austria
Medizinische Universitat Wien (Medical University of Vienna)
Vienna, Austria
CHU de Grenoble
Grenoble, France
CHRU Lille
Lille, France
Groupement Hospitalier Edouard Herriot
Lyon, France
CHU Montpellier - Hôpital St Eloi
Montpellier, France
Hôtel Dieu de Paris Hospital
Paris, France
Hôpital Saint Antoine
Paris, France
Centre Hospitalier Universitaire Hopitaux de Rouen
Rouen, France
Start Date
September 15, 2021
Primary Completion Date
June 30, 2022
Completion Date
June 30, 2022
Last Updated
January 13, 2023
207
ACTUAL participants
Lead Sponsor
Takeda
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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