[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100530883":3},{"organization":4,"armGroups":7,"interventions":13,"overallOfficials":10,"centralContacts":21,"locations":28,"responsibleParty":113,"collaborators":115,"id":118,"slug":119,"hasResults":120,"nctId":121,"briefTitle":122,"officialTitle":123,"acronym":10,"eligibilityCriteria":124,"healthyVolunteers":120,"sex":125,"minAge":10,"maxAge":126,"enrollmentInfo":127,"targetDuration":10,"studyType":130,"phases":10,"briefSummary":131,"conditions":132,"keywords":10,"overallStatus":31,"whyStopped":10,"lastUpdateSubmitDate":135,"lastUpdatePostDateStruct":136,"startDateStruct":139,"completionDateStruct":141,"leadSponsor":143,"locationsCount":144},{"fullName":5,"class":6},"Sanofi","INDUSTRY",[8],{"label":9,"type":10,"description":10,"interventionNames":11},"Olipudase alfa arm",null,[12],"Drug: Olipudase alfa",[14],{"type":15,"name":16,"description":17,"armGroupLabels":18,"otherNames":19},"DRUG","Olipudase alfa","This study will not administer any treatment, only observe the treatment as prescribed in real-world clinical practice.",[9],[20],"Xenpozyme®",[22],{"name":23,"role":24,"phone":25,"phoneExt":26,"email":27},"Trial Transparency email recommended (Toll free for US & Canada)","CONTACT","800-633-1610","option 6","contact-us@sanofi.com",[29,50,67,82,98],{"facility":30,"status":31,"city":32,"state":33,"zip":34,"country":35,"countryCode":36,"cosmosGeoPoint":37,"geoPoint":42,"contacts":43},"Ann and Robert H Lurie Children's Hospital of Chicago- Site Number: 001002","RECRUITING","Chicago","Illinois","60611","United States","US",{"type":38,"coordinates":39},"Point",[40,41],-87.65005,41.85003,{"lat":41,"lon":40},[44,48],{"name":45,"role":24,"phone":46,"phoneExt":10,"email":47},"Joshua Baker","312-227-4000","jobaker@luriechildrens.org",{"name":45,"role":49,"phone":10,"phoneExt":10,"email":10},"PRINCIPAL_INVESTIGATOR",{"facility":51,"status":31,"city":52,"state":53,"zip":54,"country":35,"countryCode":36,"cosmosGeoPoint":55,"geoPoint":59,"contacts":60},"Children's Hospital Medical Center- Site Number: 001003","Cincinnati","Ohio","45229-3039",{"type":38,"coordinates":56},[57,58],-84.51439,39.12711,{"lat":58,"lon":57},[61,65],{"name":62,"role":24,"phone":63,"phoneExt":10,"email":64},"Nicole K. Weaver","800-647-4805","Kathryn.Weaver@cchmc.org",{"name":66,"role":49,"phone":10,"phoneExt":10,"email":10},"Nicole K. Weaver, MD",{"facility":68,"status":31,"city":69,"state":53,"zip":70,"country":35,"countryCode":36,"cosmosGeoPoint":71,"geoPoint":75,"contacts":76},"Nationwide Children's Hospital - PIN- Site Number : 1001-1","Columbus","43205-2664",{"type":38,"coordinates":72},[73,74],-82.99879,39.96118,{"lat":74,"lon":73},[77,81],{"name":78,"role":24,"phone":79,"phoneExt":10,"email":80},"William Burns","614-722-3535","william.burns@nationwidechildrens.org",{"name":78,"role":49,"phone":10,"phoneExt":10,"email":10},{"facility":83,"status":31,"city":84,"state":85,"zip":86,"country":35,"countryCode":36,"cosmosGeoPoint":87,"geoPoint":91,"contacts":92},"Pulse InfoFrame US Inc.- Site Number: 001001","Philadelphia","Pennsylvania","19104",{"type":38,"coordinates":88},[89,90],-75.16362,39.95238,{"lat":90,"lon":89},[93,97],{"name":94,"role":24,"phone":95,"phoneExt":10,"email":96},"Femida Gwadry-Sridhar","519-872-1471","femida@pulseinfoframe.com",{"name":94,"role":49,"phone":10,"phoneExt":10,"email":10},{"facility":99,"status":31,"city":100,"state":101,"zip":102,"country":35,"countryCode":36,"cosmosGeoPoint":103,"geoPoint":107,"contacts":108},"Dell Children's Medical Center- Site Number : 1001-2","Austin","Texas","78723",{"type":38,"coordinates":104},[105,106],-97.74306,30.26715,{"lat":106,"lon":105},[109],{"name":110,"role":24,"phone":111,"phoneExt":10,"email":112},"James B. Gibson","512-628-1810","JBGibson@ascension.org",{"type":114,"investigatorFullName":10,"investigatorTitle":10,"investigatorAffiliation":10,"oldNameTitle":10,"oldOrganization":10},"SPONSOR",[116],{"name":117,"class":6},"Pulse Infoframe Ltd.","100530883","a-real-world-long-term-safety-and-immunogenicity-study-of-olipudase-alfa-therapy-in-pediatric-patients-less-than-2-years-of-age-with-acid-sphingomyelinase-deficiency-asmd-100530883",false,"NCT06192576","A Real-world Long-term Safety and Immunogenicity Study of Olipudase Alfa Therapy in Pediatric Patients Less Than 2 Years of Age With Acid Sphingomyelinase Deficiency (ASMD)","A Prospective Observational Study to Assess the Long-term Safety and Immunogenicity of Olipudase Alfa Therapy During Routine Clinical Care in Pediatric Patients Less Than 2 Years of Age With Acid Sphingomyelinase Deficiency","Inclusion Criteria:\n\n* The participant must have ASMD type A\u002FB or B and must be \\\u003C2 years of age at the time of treatment initiation, OR ASMD type A (without age restriction).\n* The participant must weigh ≥ 2 kg \\[The United States Prescribing Information (USPI)\\] for olipudase alfa specifies this minimum weight for infants receiving olipudase alfa).\n* The participant must have documented ASMD, as determined in peripheral leukocytes, cultured fibroblasts, or lymphocytes and\u002For by genotype determination.\n* Signed informed consent must be provided by the participant's parent(s)\u002Flegal guardian(s), including compliance with the requirements and restrictions listed in the informed consent form (ICF) and in this protocol. The signed ICF must be provided before any protocol-related procedures are performed.\n* The participant is eligible to start olipudase alfa enzyme replacement therapy or has received the first dose (and no more) of olipudase alfa, and has retrievable clinical, laboratory, and ADA data.\n\nExclusion Criteria:\n\n* The participant has received an investigational drug within 30 days or 5 drug half-lives before signature of the ICF and study enrollment.\n* The participant is not suitable for participation for reasons determined by the Investigator, including medical or clinical conditions, or potential risk of noncompliance with study procedures.\n* The participant is an immediate family member of employees of the study site or other individuals directly involved in study conduct, in conjunction with Section 1.61 of ICH-GCP Ordinance E6.","ALL","2 Years",{"count":128,"type":129},10,"ESTIMATED","OBSERVATIONAL","US, multicenter, cohort, open label observational study with primary data collection. Ancillary protocol-specified procedures to address the study objectives (eg, assessment of ADA) may be considered outside the standard of care for acid sphingomyelinase deficiency (ASMD), but the study methodology remains non-interventional, as the additional collection of data from participants will not dictate treatment. The total overall study duration will be 5 years. The follow-up period will be a minimum of 1 year to a maximum of 3 years. The enrollment period will be up to 4 years, to allow a minimum of 1 year of follow-up for the last participant enrolled.",[133,134],"Niemann-Pick Diseases","Acid Sphingomyelinase Deficiency","2025-10-30",{"date":137,"type":138},"2025-10-31","ACTUAL",{"date":140,"type":138},"2024-04-16",{"date":142,"type":129},"2029-01-15",{"name":5,"class":6},5]