[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Alice Bertaina\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":70},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,41],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100381686","stem-cell-transplant-from-donors-after-alpha-beta-cell-depletion-in-children-and-young-adults-100381686",false,"NCT04249830","Stem Cell Transplant From Donors After Alpha Beta Cell Depletion in Children and Young Adults","Allogeneic Hematopoietic Stem Cell Transplantation From an HLA-partially Matched Related or Unrelated Donor After TCR αβ+T Cells\u002FCD19+ B Cell Depletion in Children and Young Adults Affected by Malignant or Non-Malignant Hematological Disorders","Inclusion Criteria for Cohort M and Cohort NM:\n\n1. Age \\\u003C 60 years and \\> 1 month;\n2. Life expectancy \\> 10 weeks;\n3. Patients deemed eligible for allogeneic HSCT per institutional guidelines;\n4. Patients with life-threatening hematological malignancies and non-malignant disorders that could benefit from HSCT;\n\n   a. For malignant patients: i. High-risk acute lymphoblastic leukemia (ALL) in 1st complete remission (CR), ALL in 2nd CR; or ii. High-risk acute myeloid leukemia (AML) in 1st CR, AML in 2nd CR; or iii. Childhood Myelodysplastic Syndrome (MDS) with low blasts (cMDS-LB) or Childhood MDS with increased blasts (cMDS-IB); or iv. Juvenile myelomonocytic leukemia (JMML); or v. Mixed-phenotype acute leukemia (MPAL); or vi. Non-Hodgkin lymphomas in 2nd CR; or vii. Other hematologic malignancies in 1st or 2nd CR eligible for stem cell transplantation per institutional standard b. Patients with non-malignant disorders receiving first HSCT: i. using mis-matched donors, due to the absence of suitable HLA identical sibling or HLA phenotypically identical relative; or ii. whose disease put them at increased risk of graft rejection or GvHD (e.g., Fanconi Anemia, STAT1 gain of function) and therefore can benefit from receiving alpha beta depleted HSCT using as a donor either an HLA identical sibling or an HLA phenotypically identical (10\u002F10 matched) donor;\n5. A minimum genotypic identical match of 5\u002F10 is required;\n6. The donor and recipient must be identical, as determined by high resolution typing, in at least one allele of each of the following genetic loci: HLA-A, HLA-B, HLA-C, HLA-DQB1 and HLA-DRB1;\n7. Lansky\u002FKarnofsky score \\> 50; the Karnofsky Scale will be used in subjects ≥ 16 years of age, and the Lansky Scale will be used for those \\\u003C 16 years of age.\n8. All subjects ≥ 18 years of age must be able to give informed consent or adults lacking capacity to consent must have a legally authorized representative (LAR) available to provide consent. For subjects \\\u003C18 years old their legal authorized representative (LAR) (i.e. parent or guardian) must give informed consent. Pediatric subjects will be included in age appropriate discussion and written assent will be obtained for those \\> 7 years of age, when appropriate\n9. Male and female subjects of childbearing potential must agree to use an effective means of birth control to avoid pregnancy throughout the transplant procedure, while on immunosuppression, and if the subject experiences any chronic GvHD.\n\nExclusion Criteria for Cohort M and Cohort NM:\n\n1. Pregnant or lactating females;\n2. Has received a prior allogenic HSCT;\n3. Secondary MDS or AML or treatment related MDS or AML;\n4. Dysfunction of liver (ALT\u002FAST \\> 10 times upper normal value, or direct bilirubin \\> 3 times upper normal value),\n5. Serum creatinine \\> 1.5 times ULN (for patients not on dialysis) or unmanageable dysfunction of renal function while undergoing dialysis (for patients on dialysis);\n6. Severe cardiovascular disease (congestive heart failure or left ventricular ejection fraction \\\u003C 30%);\n7. Current active infectious disease (including positive HIV serology or viral RNA);\n8. Serious concurrent uncontrolled medical disorders;\n9. Lack of patient's\u002Fparents'\u002Fguardian's informed consent;\n10. Any severe concurrent disease which, in the judgement of the PI, would place the patient at increased risk during participation in the study.","ALL","1 Month","60 Years",{"count":20,"type":21},204,"ESTIMATED","INTERVENTIONAL",[24],"NA","The purpose of the CliniMACS® TCRαβ-Biotin System and CliniMACS® CD19 is to improve the safety and efficacy of allogeneic HLA-partially matched related or unrelated donors HSCT when no matched donors are available, to treat malignant and nonmalignant disorders for which HSCT is the recommended best available therapy. Initially this device will be used in a single-center, open-label, single-arm, phase II clinical trial to evaluate the efficacy of haploidentical PBSC grafts depleted of TCRα\u002Fβ+ and CD19+ cells using the CliniMACS® TCRαβ\u002FCD19 System in children and adults with hematological and non-hematological malignancies.",[27],"Hematologic Diseases","RECRUITING","2025-05-22",{"date":31,"type":32},"2025-05-29","ACTUAL",{"date":34,"type":32},"2020-02-01",{"date":36,"type":21},"2030-12",{"name":38,"class":39},"Alice Bertaina","OTHER",1,{"id":42,"slug":43,"hasResults":11,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":4,"eligibilityCriteria":47,"healthyVolunteers":11,"sex":16,"minAge":48,"maxAge":49,"enrollmentInfo":50,"targetDuration":4,"studyType":22,"phases":52,"briefSummary":55,"conditions":56,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":40},"100478287","phase-1-early-trial-of-allogeneic-hematopoietic-stem-cell-transplantation-for-patients-who-will-receive-a-kidney-transplant-from-the-same-donor-100478287","NCT05508009","Early Trial of Allogeneic Hematopoietic Stem Cell Transplantation for Patients Who Will Receive a Kidney Transplant From the Same Donor","Phase 1b\u002F2a Trial of Allogeneic Hematopoietic Stem Cell Transplantation (HSCT) From an HLA-partially Matched Related or Unrelated Donor After TCRαβ+ T-cell\u002FCD19+ B-cell Depletion for Patients Who Will Receive a Kidney Transplant (KT) From the Same HSCT\u002FKT Donor","Inclusion Criteria:\n\n* Anticipated need for kidney transplant due to:\n\n  a. Underlying genetic\u002Fimmunologic disease the following conditions i. SIOD ii. FSGS iii. Cystinosis iv. SLE v. Membranoproliferative glomerulonephritis vi. Renal vasculitis characterized by positivity of the presence of ANCA vii. Other genetic diseases leading to kidney disease requiring KT Or b. Patients who have rejected a previous KT regardless of the underlying disease\n* Chronic kidney disease (CKD) stage 3 or greater\n* Steroids \\\u003C 0.5 mg\u002FKg\u002Fday\n* The donor and recipient must be identical, as determined by high resolution typing, at least one allele of each of the following genetic loci: HLA-A, HLA-B, HLA-Cw, HLA-DQB1 and HLA-DRB1\n* Lansky\u002FKarnofsky score \\> 50; the Karnofsky Scale will be used in subjects ≥ 16 years of age, and the Lansky Scale will be used for those \\\u003C 16 years of age.\n* Able to give informed consent or have an LAR available to provide consent\n* Male and female subjects of childbearing potential must agree to use an effective means of birth control to avoid pregnancy throughout the transplant procedure, while on immunosuppression, and if the subject experiences any cGvHD\n\nExclusion Criteria:\n\n* Pregnant or lactating females.\n* Greater than Grade II aGvHD or severe, unmanaged extensive cGvHD due to a previous allograft at the time of inclusion\n* Dysfunction of liver (ALT\u002FAST \\> 10 times upper normal value, or direct bilirubin \\> 3 times upper normal value), unmanageable dysfunction of renal function while undergoing dialysis\n* Severe cardiovascular disease at the time of evaluation unresponsive to nutritional and dialytic support (left ventricular ejection fraction \\\u003C 40%), or clinical or echocardiographic evidence of severe diastolic dysfunction\n* Current active infectious disease. Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial. For patients with evidence of chronic hepatitis B virus (HBV) infection, the HBV viral load must be undetectable on suppressive therapy, if indicated. Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. Patients with HCV infection who are currently on treatment are eligible if they have an undetectable HCV viral load.\n* Serious concurrent uncontrolled medical disorders except for primary disease leading to chronic kidney disease\n* Lack of patient\u002Fparent\u002Fguardian informed consent\n* Any severe concurrent disease which, in the judgement of the investigator would place the patient at increased risk during participation in the study","1 Year","30 Years",{"count":51,"type":21},12,[53,54],"PHASE1","PHASE2","This is a single center, non-randomized, non-controlled open-label phase 1b\u002F2a trial of performing sequential αβdepleted-HSCT and KT in patients requiring KT to prevent kidney rejection post-KT, in the absence of any post-KT immunosuppression, to abrogate the need for lifelong immunosuppression, the risk of chronic rejection and, ultimately, the need for repeated transplantation.",[57,58,59,60,61],"SIOD","Cystinosis","FSGS","SLE Nephritis","CKD Stage 4","2023-07-13",{"date":64,"type":32},"2023-07-17",{"date":66,"type":32},"2023-01-10",{"date":68,"type":21},"2034-10",{"name":38,"class":39},""]