[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100610087":3},{"organization":4,"armGroups":7,"interventions":21,"overallOfficials":39,"centralContacts":43,"locations":50,"responsibleParty":120,"collaborators":122,"id":125,"slug":126,"hasResults":127,"nctId":128,"briefTitle":129,"officialTitle":130,"acronym":26,"eligibilityCriteria":131,"healthyVolunteers":127,"sex":132,"minAge":133,"maxAge":26,"enrollmentInfo":134,"targetDuration":26,"studyType":137,"phases":138,"briefSummary":140,"conditions":141,"keywords":143,"overallStatus":52,"whyStopped":26,"lastUpdateSubmitDate":144,"lastUpdatePostDateStruct":145,"startDateStruct":148,"completionDateStruct":150,"leadSponsor":152,"locationsCount":153},{"fullName":5,"class":6},"Memorial Sloan Kettering Cancer Center","OTHER",[8,16],{"label":9,"type":10,"description":11,"interventionNames":12},"Standard Fludarabine regimen followed by CAR-T","ACTIVE_COMPARATOR","Fludarabine 30 mg\u002Fm2\u002Fdose x 4 doses on days -6 to -3 (or -7 to -4)",[13,14,15],"Drug: Fludarabine","Drug: Cyclophosphamide","Biological: CAR-T",{"label":17,"type":18,"description":19,"interventionNames":20},"Targeted fludarabine regimen followed by CAR-T","EXPERIMENTAL","Fludarabine 40 mg\u002Fm2\u002Fdose x 2 doses on days -6 and -5 (or -7 and -6), with doses on days -4 and -3 (or -5 and -4, if starting lymphodepletion on day -7) adjusted based on PK analysis to target a cumulative area under the curve (AUC) of 18 mg\\*h\u002FL (range 17.5-18.5mg\\*h\u002FL",[14,13,15],[22,27,31,34],{"type":23,"name":24,"description":11,"armGroupLabels":25,"otherNames":26},"DRUG","Fludarabine",[9],null,{"type":23,"name":28,"description":29,"armGroupLabels":30,"otherNames":26},"Cyclophosphamide","All patients will receive Cyclophosphamide 500 mg\u002Fm2 IV on days -6 and -5 (or -7 and -6).",[9,17],{"type":23,"name":24,"description":32,"armGroupLabels":33,"otherNames":26},"Targeted fludarabine LD: Fludarabine 40 mg\u002Fm2\u002Fdose x 2 doses on days -6 and -5 (or\n\n-7 and -6), with doses on days -4 and -3 (or -5 and -4, if starting lymphodepletion on day -7) adjusted based on PK analysis to target a cumulative area under the curve (AUC) of 18 mg\\*h\u002FL (range 17.5-18.5mg\\*h\u002FL)",[17],{"type":35,"name":36,"description":37,"armGroupLabels":38,"otherNames":26},"BIOLOGICAL","CAR-T","will be infused based on institutional guidelines.",[9,17],[40],{"name":41,"affiliation":5,"role":42},"Kevin Curran, MD","PRINCIPAL_INVESTIGATOR",[44,48],{"name":41,"role":45,"phone":46,"phoneExt":26,"email":47},"CONTACT","1-833-MSK-KIDS","currank@mskcc.org",{"name":49,"role":45,"phone":46,"phoneExt":26,"email":26},"Jaap Jan Boelens, MD, PhD",[51,68,82,96,111],{"facility":5,"status":52,"city":53,"state":53,"zip":54,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"RECRUITING","New York","10065","United States","US",{"type":58,"coordinates":59},"Point",[60,61],-74.00597,40.71427,{"lat":61,"lon":60},[64,65,67],{"name":41,"role":45,"phone":46,"phoneExt":26,"email":26},{"name":66,"role":45,"phone":46,"phoneExt":26,"email":26},"Jaap Jan Boelens, MD,PhD",{"name":41,"role":42,"phone":26,"phoneExt":26,"email":26},{"facility":69,"status":52,"city":70,"state":71,"zip":72,"country":55,"countryCode":56,"cosmosGeoPoint":73,"geoPoint":77,"contacts":78},"Cincinnati Children's Hospital Medical Center (Data Collection Only)","Cincinnati","Ohio","45229",{"type":58,"coordinates":74},[75,76],-84.51439,39.12711,{"lat":76,"lon":75},[79],{"name":80,"role":45,"phone":81,"phoneExt":26,"email":26},"Christine Phillips, MD","513-636-4266",{"facility":83,"status":52,"city":84,"state":85,"zip":86,"country":55,"countryCode":56,"cosmosGeoPoint":87,"geoPoint":91,"contacts":92},"Children's Hospital of Philadelphia (Data Collection Only)","Philadelphia","Pennsylvania","19104",{"type":58,"coordinates":88},[89,90],-75.16362,39.95238,{"lat":90,"lon":89},[93],{"name":94,"role":45,"phone":95,"phoneExt":26,"email":26},"Regina Myers, MD","267-426-0762",{"facility":97,"status":98,"city":99,"state":100,"zip":101,"country":55,"countryCode":56,"cosmosGeoPoint":102,"geoPoint":106,"contacts":107},"Baylor College Medical Center (Data Collection Only)","NOT_YET_RECRUITING","Houston","Texas","77030",{"type":58,"coordinates":103},[104,105],-95.36327,29.76328,{"lat":105,"lon":104},[108],{"name":109,"role":45,"phone":26,"phoneExt":26,"email":110},"Rayne Rouce, MD","rouce@bcm.edu",{"facility":112,"status":98,"city":99,"state":100,"zip":101,"country":55,"countryCode":56,"cosmosGeoPoint":113,"geoPoint":115,"contacts":116},"Texas Children's Hospital (Data Collection)",{"type":58,"coordinates":114},[104,105],{"lat":105,"lon":104},[117],{"name":118,"role":45,"phone":119,"phoneExt":26,"email":26},"Rayne Rouce, M.D., B.S.","832-822-4242",{"type":121,"investigatorFullName":26,"investigatorTitle":26,"investigatorAffiliation":26,"oldNameTitle":26,"oldOrganization":26},"SPONSOR",[123],{"name":124,"class":6},"Princess Maxima Center for Pediatric Oncology","100610087","phase-3-a-study-of-fludarabine-dosing-in-children-and-young-adults-with-b-cell-acute-lymphoblastic-leukemia-100610087",false,"NCT07223021","A Study of Fludarabine Dosing in Children and Young Adults With B-cell Acute Lymphoblastic Leukemia","Improving EveNt Free Survival by Optimizing FLUdarabine Exposure During LymphodepletioN for CAR T CEll Therapy: a Randomized, Multi-center Study of Children and Young Adults With B-cell Acute Lymphoblastic Leukemia (INFLUENCE)","Inclusion Criteria:\n\n* Patients with B-ALL and eligible to receive commercial tisagenlecleucel.\n* Patient's weight \\> 9 kg at time of lymphodepleting chemotherapy\n* Adequate organ function at time of LD is required and is defined:\n\n  * Hepatic: Serum bilirubin ≤ 2 mg\u002FdL, unless benign congenital hyperbilirubinemia\n  * Hepatic: AST and ALT \\\u003C 5x the upper limit of normal for age, unless thought to be leukemic disease-related\n  * Renal: Calculated glomerular filtration rate (GFR) ≥ 70 ml\u002Fmin\u002F1.73m\\^2. (based on Schwartz formula GFR (mL\u002Fmin\u002F1.73 m²) = (36.2 × Height in cm) \u002F Creatinine in mg\u002FdL\n  * Cardiac: LVEF ≥ 50% by multi-gated acquisition scan (MUGA), resting echocardiogram, or cardiac magnetic resonance imaging (MRI) within 6 weeks of screening\n  * Pulmonary: Oxygen saturation as recorded by pulse oximetry of ≥ 90% on room air\n* Adequate performance status:\n\n  * Age ≥ 16 years: ECOG ≤ 1 or Karnofsky \\> 60% at treatment\n  * Age \\\u003C 16 years: Lansky ≥ 60% at treatment\n* Willing to participate as research subject and provide written informed consent from parents\u002Flegal representative, patient, and age-appropriate assent as appropriate before any study specific screening procedures are conducted, according to local, regional or national law and legislation.\n\nExclusion Criteria:\n\n* Have a known immediate or delayed hypersensitivity reaction or idiosyncrasy to the study drugs, or drugs chemically related to study treatment or excipients that contraindicate their participation, including fludarabine, cyclophosphamide and tisagenlecleucel.\n* Patients with tisagenlecleucel that is deemed out of specification (OOS) will be excluded from this protocol\n* Clinically significant active and uncontrolled infection confirmed by clinical evidence, imaging, or positive laboratory tests (e.g., blood cultures, PCR for DNA\u002FRNA etc.)\n* Patient\u002Fparent\u002Fguardian unable to give informed consent or unable to comply with the treatment protocol.\n* Pregnant or lactating women","ALL","1 Year",{"count":135,"type":136},130,"ESTIMATED","INTERVENTIONAL",[139],"PHASE3","The researchers are doing this study to find out whether PK-targeted fludarabine is an effective Lymphodepletion (LD) chemotherapy approach for people with relapsed\u002Frefractory B-cell acute lymphoblastic leukemia (B-ALL) who will receive tisagenlecleucel CAR T-cell therapy. The researchers will compare PK-targeted fludarabine dosing with standard fludarabine dosing to see which treatment approach is more effective. The researchers will also look at whether PK-targeted fludarabine dosing is feasible (practical), the side effects of the study treatment, and how the study treatment affects people's quality of life. The researchers will measure quality of life by having participants complete questionnaires.",[142],"B-cell Acute Lymphoblastic Leukemia",[24],"2026-06-11",{"date":146,"type":147},"2026-06-12","ACTUAL",{"date":149,"type":147},"2025-10-20",{"date":151,"type":136},"2028-10",{"name":5,"class":6},5]