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Clinical Trial Summary

Current standard therapy for patients with haemophilia (PwH) in the prevention of bleeding episodes is a prophylactic intravenous treatment with recombinant coagulation factor (F) VIII (Haemophilia A) or rather FIX (Haemophilia B) two to three times weekly. With the development of recombinant factor VIII Fc fusion protein (rFVIIIFc) the conventional routine prophylaxis regime is complemented by an extended half-life (EHL) factor replacement prophylaxis with the potential of improved bleed prevention and reduced injection frequency at similar factor consumption. Aim of this longitudinal multicentre study is to evaluate the influence of an EHL factor replacement regime with rFVIIIFc on haemophilic specific parameters (annual bleeding rate, bleeding localisation), joint status, pain, functional parameters, treatment adherence and health-related quality of life in PwH A.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04583930
Study type Observational
Source University of Wuppertal
Contact Thomas Hilberg, Prof.
Phone 004920237320812
Email hilberg@uni-wuppertal.de
Status Recruiting
Phase
Start date February 1, 2021
Completion date April 20, 2023

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