[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100624054":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":24,"centralContacts":28,"locations":34,"responsibleParty":47,"collaborators":10,"id":49,"slug":50,"hasResults":51,"nctId":52,"briefTitle":53,"officialTitle":54,"acronym":10,"eligibilityCriteria":55,"healthyVolunteers":51,"sex":56,"minAge":10,"maxAge":57,"enrollmentInfo":58,"targetDuration":10,"studyType":61,"phases":10,"briefSummary":62,"conditions":63,"keywords":65,"overallStatus":37,"whyStopped":10,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":71,"leadSponsor":73,"locationsCount":74},{"fullName":5,"class":6},"Takeda","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"vonicog alfa (rVWF) Group",null,"Participants with Von Willebrand Disease (vWD) who received vonicog alfa (rVWF) in accordance with package insert.",[13],"Drug: vonicog alfa (rVWF)",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"DRUG","vonicog alfa (rVWF)","rVWF administered by intravenous injection.",[9],[21,22,23],"Vonvendi Intravenous","Recombinant von Willebrand Factor (rVWF)","TAK-577",[25],{"name":26,"affiliation":5,"role":27},"Study Director","STUDY_DIRECTOR",[29],{"name":30,"role":31,"phone":32,"phoneExt":10,"email":33},"Takeda Contact","CONTACT","+1-877-825-3327","medinfoUS@takeda.com",[35],{"facility":36,"status":37,"city":38,"state":38,"zip":10,"country":39,"countryCode":40,"cosmosGeoPoint":41,"geoPoint":46,"contacts":10},"Takeda selected site","RECRUITING","Tokyo","Japan","JP",{"type":42,"coordinates":43},"Point",[44,45],139.69171,35.6895,{"lat":45,"lon":44},{"type":48,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100624054","an-observational-study-of-vonicog-alfa-rvwf-in-pediatric-participants-with-von-willebrand-disease-vwd-100624054",false,"NCT07404644","An Observational Study of Vonicog Alfa (rVWF) in Pediatric Participants With Von Willebrand Disease (vWD)","Vonvendi Intravenous Specified Drug Use-results Survey \"Pediatric Administration\"","Inclusion Criteria :\n\n* Under 18 years old with vWD.\n* Participants who are treated with rVWF for the purpose of hemostatic treatment and management during bleeding episodes or perioperative periods.\n* Participants who have prescription or administration after the approval date of rVWF for pediatric use in Japan.\n\nExclusion Criteria :\n\n\\- Patients who are participating in clinical trials of rVWF.","ALL","17 Years",{"count":59,"type":60},13,"ESTIMATED","OBSERVATIONAL","This study is conducted in Japan of vonicog alfa (rVWF) used to treat pediatric participants with Von Willebrand Disease (vWD).\n\nThe main aim of the study is to evaluate adverse drug reaction and effectiveness of vonicog alfa (rVWF).\n\nDuring the study, pediatric participants with vWD will be administered with rVWF under routine normal practice. The investigators will evaluate adverse events due to rVWF for 1 year from the start of drug administration.\n\nThe study sponsor will not be involved in how the participants are administered but will be recorded what happens during the study.",[64],"Von Willebrand Disease (vWD)",[64],"2026-02-19",{"date":68,"type":69},"2026-02-23","ACTUAL",{"date":66,"type":69},{"date":72,"type":60},"2031-05-30",{"name":5,"class":6},1]