[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"hematologic-disease\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:hematologic-disease":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,46],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":15,"eligibilityCriteria":16,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":4,"studyType":23,"phases":24,"briefSummary":26,"conditions":27,"keywords":29,"overallStatus":33,"whyStopped":4,"lastUpdateSubmitDate":34,"lastUpdatePostDateStruct":35,"startDateStruct":38,"completionDateStruct":40,"leadSponsor":42,"locationsCount":45},"100578316","phase-1-human-leukocyte-antigen-hla-mismatched-unrelated-allogeneic-hematopoietic-stem-cell-transplantation-100578316",false,"NCT06809712","Human Leukocyte Antigen (HLA) Mismatched Unrelated Allogeneic Hematopoietic Stem Cell Transplantation","A Prospective Single-arm Trial on Human Leukocyte Antigen (HLA) Mismatched Unrelated Allogeneic Hematopoietic Stem Cell Transplantation","MIGHT","Inclusion Criteria:\n\n* Adult patients (18-60 years old) with hematological malignancies and indications for hematopoietic stem cell transplantation;\n* Non blood donors without human leukocyte antigen (HLA) high-resolution typing ≥ 9\u002F10, or those who have difficulty finding non blood donors due to urgent medical conditions;\n* No suitable HLA matching haploidentical donor available;\n* There are suitable unrelated HLA mismatched (HLA high-resolution typing\\\u003C9\u002F10) donors;\n* The subjects or their legal representatives shall sign an informed consent form before the start of the clinical study.\n\nExclusion Criteria:\n\n* Patients with severe liver and kidney function (alanine aminotransferase\\>2.5 times the upper limit of normal, blood creatinine\\>1.5 times the upper limit of normal) and cardiopulmonary dysfunction (New York Heart Association (NYHA) III\u002FIV heart function, ejection fraction\\\u003C50%, severe obstructive or restrictive ventilation dysfunction);\n* Merge active infections;\n* Eastern Cooperative Oncology Group Performance Status (ECOG) score ≥ 2 points;\n* Secondary tumors with merged activity;\n* Severe central nervous system or mental illness leading to the inability to autonomously choose to enter or exit clinical trials;\n* Combine other allo hematopoietic stem cell transplantation (HSCT) contraindications.","ALL","18 Years","60 Years",{"count":21,"type":22},29,"ESTIMATED","INTERVENTIONAL",[25],"PHASE1","This study is a single center, prospective, single arm exploratory clinical trial that includes patients with hematological malignancies who are indicated for allogeneic hematopoietic stem cell transplantation (allo HSCT) but lack suitable donors. This project plans to use highly mismatched unrelated HLA mismatched donors. Ultimately, an unrelated human leukocyte antigen (HLA) mismatched allo HSCT transplantation plan will be established to improve the disease prognosis of this group of patients and truly enter the era of \"everyone has a donor\" for allo HSCT.",[28],"Hematologic Disease",[30,31,32],"Hematopoietic cell transplantation","HLA mismatch","Hematologic diseases","RECRUITING","2026-06-05",{"date":36,"type":37},"2026-06-09","ACTUAL",{"date":39,"type":37},"2022-08-04",{"date":41,"type":22},"2027-10-31",{"name":43,"class":44},"He Huang","OTHER",1,{"id":47,"slug":48,"hasResults":11,"nctId":49,"briefTitle":50,"officialTitle":50,"acronym":4,"eligibilityCriteria":51,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":52,"targetDuration":4,"studyType":23,"phases":54,"briefSummary":56,"conditions":57,"keywords":58,"overallStatus":61,"whyStopped":4,"lastUpdateSubmitDate":62,"lastUpdatePostDateStruct":63,"startDateStruct":65,"completionDateStruct":67,"leadSponsor":69,"locationsCount":4},"100580898","universal-genetic-testing-of-patients-with-hematological-malignancies-ugt-100580898","NCT06843291","UNIVERSAL GENETIC TESTING OF PATIENTS WITH HEMATOLOGICAL MALIGNANCIES (UGT)","Inclusion Criteria:\n\n\\- a. Age ≥ 18 years of age. b. A new diagnosis of HM. c. Diagnostic bone marrow to be performed at Wellstar MCG Health\u002FGeorgia Cancer Center.\n\nd. Ability and willingness to provide informed consent in English to undergo skin biopsy for fibroblast culture and NGS for comparison with the BM NGS.\n\nExclusion Criteria:\n\n* There are no exclusion criteria.",{"count":53,"type":22},100,[55],"NA","We propose to perform NGS and OGM with DNA extracted from bone marrow (BM; site of cancer) and NGS on skin fibroblast DNA (proxy for germline) on all patients with hematologic malignancies (HM) who undergo a standard-of-care BM biopsy at Georgia Cancer Center\u002FWellstar MCG Health. Simultaneous 4 mm punch skin biopsy for fibroblast culture will be obtained at the planned puncture site of the BM biopsy. The bone marrow biopsy and aspirate are already part of the patient's scheduled medical evaluation and the punch biopsy of the skin is the only additional procedure involved in the study.",[28],[59,60],"Genetic testing","hematological malignancies","NOT_YET_RECRUITING","2025-02-20",{"date":64,"type":37},"2025-02-24",{"date":66,"type":22},"2025-02",{"date":68,"type":22},"2029-02",{"name":70,"class":44},"Augusta University"]