[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100550016":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":32,"responsibleParty":45,"collaborators":10,"id":47,"slug":48,"hasResults":49,"nctId":50,"briefTitle":51,"officialTitle":52,"acronym":10,"eligibilityCriteria":53,"healthyVolunteers":49,"sex":54,"minAge":10,"maxAge":10,"enrollmentInfo":55,"targetDuration":10,"studyType":58,"phases":10,"briefSummary":59,"conditions":60,"keywords":10,"overallStatus":35,"whyStopped":10,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":66,"completionDateStruct":68,"leadSponsor":70,"locationsCount":71},{"fullName":5,"class":6},"Takeda","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Recombinant ADAMTS13",null,"Participants will receive recombinant ADAMTS13 intravenous injection.",[13],"Drug: Recombinant ADAMTS13",[15],{"type":16,"name":9,"description":17,"armGroupLabels":18,"otherNames":19},"DRUG","Recombinant ADAMTS13, Intravenous injection",[9],[20,21],"ADZYNMA Intravenous 1500","TAK-755",[23],{"name":24,"affiliation":5,"role":25},"Study Director","STUDY_DIRECTOR",[27],{"name":28,"role":29,"phone":30,"phoneExt":10,"email":31},"Takeda Contact","CONTACT","+1-877-825-3327","medinfoUS@takeda.com",[33],{"facility":34,"status":35,"city":36,"state":10,"zip":10,"country":37,"countryCode":38,"cosmosGeoPoint":39,"geoPoint":44,"contacts":10},"Takeda selected site","RECRUITING","Tokyo","Japan","JP",{"type":40,"coordinates":41},"Point",[42,43],139.69171,35.6895,{"lat":43,"lon":42},{"type":46,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR","100550016","a-survey-of-recombinant-adamts13-in-participants-with-congenital-thrombotic-thrombocytopenic-purpura-100550016",false,"NCT06441578","A Survey of Recombinant ADAMTS13 in Participants With Congenital Thrombotic Thrombocytopenic Purpura","Special Drug Use Surveillance of ADZYNMA Intravenous 1500 (All-Case Investigation)","Inclusion Criteria:\n\n\\- All participants with congenital thrombotic thrombocytopenic purpura (cTTP), treated with recombinant ADAMTS13\n\nExclusion Criteria:\n\n\\- None","ALL",{"count":56,"type":57},40,"ESTIMATED","OBSERVATIONAL","This study is a survey in Japan of recombinant ADAMTS13 used to treat or to prevent participants with congenital thrombotic thrombocytopenic purpura (cTTP). The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study.\n\nThe main aim of the study is to check for side effects related from recombinant ADAMTS13 and to check if recombinant ADAMTS13 improves or prevents cTTP.\n\nDuring the study, participants with cTTP will take recombinant ADAMTS13 intravenous injection according to their clinic's standard practice. The study doctors will check for side effects from recombinant ADAMTS13 for 18 months.",[61],"Thrombotic Thrombocytopenic Purpura (TTP)","2025-10-02",{"date":64,"type":65},"2025-10-07","ACTUAL",{"date":67,"type":65},"2024-05-30",{"date":69,"type":57},"2032-09-30",{"name":5,"class":6},1]