Hemostase Clinique - Institut Cœur-Poumons (4eme étage aile est) Bureau 419

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Trial	Conditions	Status	Phase	Updated	More info	NCT ID
A Study of Vonicog Alfa (rVWF) in Children With Severe Von Willebrand Disease (vWD)	Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Hemic and Lymphatic Diseases, blood coagulation disease, blood platelet disease, coagulation protein disease, hematologic disorder, hemorrhagic disease, hereditary disease, inherited blood coagulation disorder, von Willebrand disease (hereditary or acquired)	Recruiting	Phase 3	2026-09-09		NCT05582993

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