[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100642358":3},{"organization":4,"armGroups":7,"interventions":8,"overallOfficials":7,"centralContacts":13,"locations":7,"responsibleParty":23,"collaborators":7,"id":25,"slug":26,"hasResults":27,"nctId":28,"briefTitle":29,"officialTitle":30,"acronym":7,"eligibilityCriteria":31,"healthyVolunteers":27,"sex":32,"minAge":33,"maxAge":7,"enrollmentInfo":34,"targetDuration":7,"studyType":37,"phases":7,"briefSummary":38,"conditions":39,"keywords":7,"overallStatus":41,"whyStopped":7,"lastUpdateSubmitDate":42,"lastUpdatePostDateStruct":43,"startDateStruct":46,"completionDateStruct":48,"leadSponsor":50,"locationsCount":7},{"fullName":5,"class":6},"Weizmann Institute of Science","OTHER",null,[9],{"type":10,"name":11,"description":12,"armGroupLabels":7,"otherNames":7},"DIAGNOSTIC_TEST","PERIBLOOD-MPN","Observational intervation of cHSPCs",[14,19],{"name":15,"role":16,"phone":17,"phoneExt":7,"email":18},"Liran Shlush, Prof.","CONTACT","+97289342247","liran.shlush@weizmann.ac.il",{"name":20,"role":16,"phone":21,"phoneExt":7,"email":22},"Gil Gonen Yaacovi, PhD","+9728747027401","gil.gonen-yaacovi@weizmann.ac.il",{"type":24,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100642358","replacing-bone-marrow-diagnostics-with-peripheral-blood-analysis-in-mpn-patients-100642358",false,"NCT07648433","Replacing Bone Marrow Diagnostics With Peripheral Blood Analysis in MPN Patients","Development of a Peripheral Blood Assay to Replace Bone Marrow Biopsy in Myeloproliferative Neoplasms- a Multi-center Observational Study","Inclusion Criteria:\n\n1. Age ≥ 18 years\n2. Confirmed MPN diagnosis, based on the WHO criteria (Barbui 2018), which includes:\n\n   Polycythemia Vera (PV) Criteria:\n   * Elevated hemoglobin (\\>16.5 g\u002FdL for men, \\>16.0 g\u002FdL for women), hematocrit (\\>49% for men, \\>48% for women), or increased red cell mass\n   * Bone marrow biopsy showing hypercellularity with trilineage growth (panmyelosis)\n   * Presence of JAK2 mutation (V617F or exon 12)\n\n   Essential Thrombocythemia (ET) Criteria:\n   * Platelet count ≥450 ×10⁹\u002FL\n   * Bone marrow biopsy showing proliferation mainly of the megakaryocyte lineage\n   * Not meeting WHO criteria (Alaggio et al., 2022) for other myeloid neoplasms (such as CML, PV, PMF, MDS).\n   * Presence of JAK2, CALR, or MPL mutation Primary Myelofibrosis (PMF) Criteria\n   * Megakaryocytic proliferation and atypia, with or without reticulin fibrosis, and increased marrow cellularity (for prefibrotic\u002Fearly PMF) or significant reticulin\u002Fcollagen fibrosis (for overt PMF)\n   * Not meeting criteria for other myeloid neoplasms\n   * Presence of JAK2, CALR, or MPL mutation, or in their absence, another clonal marker\n3. Patients who are referred for a bone marrow biopsy due to a suspected diagnosis of MPN\n\nExclusion Criteria:\n\n1. Patients diagnosed with MPN receiving therapy\n2. Patients who have undergone a bone marrow transplant","ALL","18 Years",{"count":35,"type":36},500,"ESTIMATED","OBSERVATIONAL","This observational, multi-center study aims to collect data to develop a novel, minimally invasive diagnostic tool for myeloproliferative neoplasms (MPN) based on peripheral blood (PB) profiling of circulating hematopoietic stem and progenitor cells (cHSPCs) using single-cell RNA sequencing (scRNA-seq). Current diagnostic practice relies on bone marrow (BM) biopsy, procedures that is invasive, technically demanding, and may be inconclusive in early or prefibrotic disease stages.\n\nOur prior work established a reference atlas of healthy cHSPC subtypes and a computational pipeline capable of identifying disease-specific transcriptional changes by quantifying deviations from this reference. This study will assess whether PB-based genomic profiling can accurately distinguish MPN from non-clonal cytoses, including secondary erythrocytosis or thrombocytosis.\n\nPatients referred for bone marrow biopsy due to suspected myeloproliferative neoplasm (MPN) will undergo PB collection for genomic profiling. The study's primary objective is to develop a PB-based test by comparing the developed test diagnoses to the conventional BM-based diagnostics. Secondary objectives include evaluating its potential for MPN subtype classification, risk stratification, as well as assessing its ability to reduce the need for BM biopsies.",[40],"Myeloproliferative Neoplasm","NOT_YET_RECRUITING","2026-06-09",{"date":44,"type":45},"2026-06-15","ACTUAL",{"date":47,"type":36},"2026-06",{"date":49,"type":36},"2032-06",{"name":5,"class":6}]