RecruitingNCT06008938
An Observational Cohort Study to Characterize the Effectiveness and Safety of HEMGENIX® in Patients With Hemophilia B
Studying Hemophilia B
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- CSL Behring
- Principal Investigator
- Global Program DirectorCSL Behring
- Intervention
- HEMGENIX(genetic)
- Enrollment
- 500 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2023 – 2043
Study locations (12)
- American Thrombosis and Hemostasis Network, Rochester, New York, United States
- Medical University Vienna, Vienna, Austria
- Aarhus Universitetshospital, Århus N, Denmark
- Centre Hospitalier Universitaire de Brest / CHU Morvan, Brest, France
- Centre Régional de Traitement de l'Hémophilie, Nantes, France
- CHU Nancy - Hôpital Brabois, Vandœuvre-lès-Nancy, France
- Klinik für Angiologie/ Hämostaseologie, Berlin, Germany
- University of Clinic Bonn, Bonn, Germany
- Klinikum der Johann-Wolfgang Goethe Universitaet, Frankfurt, Germany
- Hannover Medical School, Hanover, Germany
- Hospital Alvaro Cunqueiro Dr. Manuel Rodriquez-Lopez, Vigo, Spain
- University Hospital Bern Inselspital, Bern, Switzerland
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.
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