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TrialConditionsStatusPhaseUpdatedMore infoNCT ID
An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With 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)RecruitingNot stated2026-02-23NCT07404644

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OrganizationsLinked trials
Takeda163

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Research sitesCityCountryLinked trials
Takeda selected siteTokyoJapan9