[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100485522":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":18,"centralContacts":19,"locations":18,"responsibleParty":25,"collaborators":18,"id":27,"slug":28,"hasResults":29,"nctId":30,"briefTitle":31,"officialTitle":32,"acronym":18,"eligibilityCriteria":33,"healthyVolunteers":29,"sex":34,"minAge":35,"maxAge":18,"enrollmentInfo":36,"targetDuration":18,"studyType":39,"phases":40,"briefSummary":42,"conditions":43,"keywords":18,"overallStatus":45,"whyStopped":18,"lastUpdateSubmitDate":46,"lastUpdatePostDateStruct":47,"startDateStruct":50,"completionDateStruct":52,"leadSponsor":54,"locationsCount":18},{"fullName":5,"class":6},"Institut Paoli-Calmettes","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"experimental:Acute leukemia\u002Fmyelodysplastic or myeloproliferative disease","EXPERIMENTAL","blood sampling, bone marrow aspirate, and buccal swab",[13],"Other: experimental:Acute leukemia\u002Fmyelodysplastic or myeloproliferative disease",[15],{"type":6,"name":9,"description":16,"armGroupLabels":17,"otherNames":18},"blood sampling, bone marrow aspirate and buccal swab",[9],null,[20],{"name":21,"role":22,"phone":23,"phoneExt":18,"email":24},"Dominique GENRE, MD","CONTACT","+33491223778","drci.up@ipc.unicancer.fr",{"type":26,"investigatorFullName":18,"investigatorTitle":18,"investigatorAffiliation":18,"oldNameTitle":18,"oldOrganization":18},"SPONSOR","100485522","collection-of-sequential-samples-from-patients-with-malignant-myeloid-hemopathy-for-the-study-of-treatment-resistance-100485522",false,"NCT05602168","Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance","Collection of Sequential Samples From Patients With Malignant Myeloid Hemopathy for the Study of Treatment Resistance: HEMATOBIO.02-IPC 2021-061","Inclusion Criteria:\n\n1. Diagnosis of acute leukemia, myelodysplastic syndrome, chronic myelomonocytic leukemia (CMML) or myeloproliferative syndrome according to the WHO classification 2016,\n2. Patient for whom a new line of therapy is initiated.\n3. Patient older than 18 years of age.\n4. Patient affiliated to the social security system or benefiting from such a system.\n5. Signed consent to participate.\n\nExclusion Criteria:\n\n1. Weight at inclusion \\\u003C 50 kg\n2. Participating in another clinical study that would cause the total amount of blood collection to exceed the and endanger the patient\n3. Person in an emergency situation, adult under legal protection (guardianship, curatorship, etc.) protection (guardianship, curatorship or safeguard of justice), or unable to express his or her consent.\n4. Impossibility to submit to the medical follow-up of the trial for geographical social or psychological reasons,\n5. Pregnant or breastfeeding women","ALL","18 Years",{"count":37,"type":38},400,"ESTIMATED","INTERVENTIONAL",[41],"NA","The main objective is to study the genomic, transcriptomic, proteomic epigenomic, metabolomic and immune mechanisms of blasts and microenvironment cells associated with IT resistance through the constitution of a collection associating blood or marrow samples from patients with LA, MDS and MPS marrow samples from patients with LA, MDS and MPS at diagnosis, during treatment and at relapse and relapse and clinical annotations.",[44],"Hematologic Cancer","NOT_YET_RECRUITING","2022-10-26",{"date":48,"type":49},"2022-11-01","ACTUAL",{"date":51,"type":38},"2023-01",{"date":53,"type":38},"2030-01",{"name":5,"class":6}]