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TrialConditionsStatusPhaseUpdatedMore infoNCT 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)RecruitingPhase 32026-09-09NCT05582993