[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100626574":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":19,"centralContacts":20,"locations":26,"responsibleParty":43,"collaborators":19,"id":45,"slug":19,"hasResults":46,"nctId":47,"briefTitle":48,"officialTitle":49,"acronym":19,"eligibilityCriteria":50,"healthyVolunteers":46,"sex":51,"minAge":19,"maxAge":52,"enrollmentInfo":53,"targetDuration":19,"studyType":56,"phases":57,"briefSummary":59,"conditions":60,"keywords":62,"overallStatus":29,"whyStopped":19,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":75},{"fullName":5,"class":6},"Sinocelltech Ltd.","INDUSTRY",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"SCT800 prophylaxis and control of bleeding events","EXPERIMENTAL","For prophylaxis, 15-50 IU\u002Fkg SCT800 is intravenously. For control of bleeding events(BE), 10-20 IU\u002Fkg for mild BE, 15 -30IU\u002Fkg for moderate BE, 30-50IU\u002Fkg for severe BE.",[13],"Drug: SCT800 prophylaxis and treatment for bleeding events",[15],{"type":16,"name":17,"description":11,"armGroupLabels":18,"otherNames":19},"DRUG","SCT800 prophylaxis and treatment for bleeding events",[9],null,[21],{"name":22,"role":23,"phone":24,"phoneExt":19,"email":25},"Runhui Wu","CONTACT","+86-13370115037","wurunhuigcp@163.com",[27],{"facility":28,"status":29,"city":30,"state":31,"zip":32,"country":33,"cosmosGeoPoint":34,"geoPoint":39,"contacts":40},"Beijing children's hospital","RECRUITING","Beijing","Beijing Municipality","000000","China",{"type":35,"coordinates":36},"Point",[37,38],116.39723,39.9075,{"lat":38,"lon":37},[41],{"name":22,"role":23,"phone":42,"phoneExt":19,"email":25},"86-13512078851",{"type":44,"investigatorFullName":19,"investigatorTitle":19,"investigatorAffiliation":19,"oldNameTitle":19,"oldOrganization":19},"SPONSOR","100626574",false,"NCT07437404","Efficacy and Safety Evaluation Study of SCT800 in Previously Untreated Hemophilia A Patients.","An Open Label, Uncontrolled Study to Evaluate the the Safety and Efficacy of SCT800 for Prophylaxis Treatment in Severe Previously Untreated Hemophilia Patients.","Inclusion Criteria:\n\n* Male subjects with severe hemophilia A (FVIII:C \\\u003C 1% in central laboratory tests)\n* previously untreated with pdFVIII\u002FrFVIII, including marketed SCT800 (those who have previously used ≤5EDs of blood products such as cryoprecipitate or fresh frozen plasma are acceptable).\n* FVIII inhibitor negative\n* informed consent.\n\nExclusion Criteria:\n\n* Known allergy to recombinant coagulation factor VIII concentrate or any excipient; known allergy to bovine, rodent or hamster bovine;\n* subjects with a history or family history of FVIII inhibitor formation;\n* Clinical liver function test (ALT、AST) ≥ 5 ULN or clinical kidney function test (BUN，Cr) ≥2 ULN;\n* Patients with other coagulation dysfunction diseases in addition to hemophilia A.\n* International Normalized Ratio (INR) \\> 1.5.","MALE","6 Years",{"count":54,"type":55},36,"ESTIMATED","INTERVENTIONAL",[58],"PHASE3","This is an Open Label, Uncontrolled Study to Evaluate the the Safety and Efficacy of SCT800 for Prophylaxis Treatment in Severe Previously Untreated Hemophilia Patients.",[61],"Haemophilia A",[63,64,65],"SCT800","haemophilia A","previously untreated patients","2026-02-23",{"date":68,"type":69},"2026-02-27","ACTUAL",{"date":71,"type":69},"2024-04-26",{"date":73,"type":55},"2028-12-26",{"name":5,"class":6},1]