[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100643635":3},{"organization":4,"armGroups":7,"interventions":16,"overallOfficials":31,"centralContacts":35,"locations":41,"responsibleParty":58,"collaborators":22,"id":60,"slug":22,"hasResults":61,"nctId":62,"briefTitle":63,"officialTitle":63,"acronym":64,"eligibilityCriteria":65,"healthyVolunteers":61,"sex":66,"minAge":67,"maxAge":68,"enrollmentInfo":69,"targetDuration":22,"studyType":72,"phases":73,"briefSummary":75,"conditions":76,"keywords":78,"overallStatus":83,"whyStopped":22,"lastUpdateSubmitDate":84,"lastUpdatePostDateStruct":85,"startDateStruct":88,"completionDateStruct":90,"leadSponsor":92,"locationsCount":93},{"fullName":5,"class":6},"UNC Lineberger Comprehensive Cancer Center","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"KMT2A-translocated (KMT2Ar) acute myeloid leukemia (AML)","EXPERIMENTAL","Patients with KMT2A-translocated (KMT2Ar) acute myeloid leukemia (AML) did not receive a treatment.",[13,14,15],"Drug: Azacitidine","Drug: Venetoclax","Drug: Revumenib",[17,23,27],{"type":18,"name":19,"description":20,"armGroupLabels":21,"otherNames":22},"DRUG","Azacitidine","Subcutaneous or IV over 10-40 minutes on Days 1-7 or days 1-5, 8-9, in every 28 days, for 3 cycles.",[9],null,{"type":18,"name":24,"description":25,"armGroupLabels":26,"otherNames":22},"Venetoclax","Per oral, daily in combination with posaconazole for 1- 28 days, for 3 cycles.",[9],{"type":18,"name":28,"description":29,"armGroupLabels":30,"otherNames":22},"Revumenib","Per oral,12 hours in combination with posaconazole for 1- 28 days , for 3 cycles.",[9],[32],{"name":33,"affiliation":5,"role":34},"Joshua Zeidner, MD","PRINCIPAL_INVESTIGATOR",[36],{"name":37,"role":38,"phone":39,"phoneExt":22,"email":40},"Lauren Higgins","CONTACT","919-984-0000","Lauren_Higgins@med.unc.edu",[42],{"facility":43,"status":22,"city":44,"state":45,"zip":46,"country":47,"cosmosGeoPoint":48,"geoPoint":53,"contacts":54},"Lineberger Comprehensive Cancer Center at University of North Carolina - Chapel Hill","Chapel Hill","North Carolina","27599-7295","United States",{"type":49,"coordinates":50},"Point",[51,52],-79.05584,35.9132,{"lat":52,"lon":51},[55,56],{"name":37,"role":38,"phone":39,"phoneExt":22,"email":40},{"name":57,"role":34,"phone":22,"phoneExt":22,"email":22},"Joshua Zeidner",{"type":59,"investigatorFullName":22,"investigatorTitle":22,"investigatorAffiliation":22,"oldNameTitle":22,"oldOrganization":22},"SPONSOR","100643635",false,"NCT07605949","Revumenib, Azacitidine, and VENetoclax in Newly Diagnosed KMT2A-Rearranged AML","RAVEN","Inclusion Criteria:\n\n* Written informed consent obtained to participate in the study and HIPAA authorization for release of personal health information.\n* Subject is willing and able to comply with study procedures based on the judgement of the investigator or protocol designee.\n* Age 18-65 years at the time of consent.\n* Untreated AML based on 2022 WHO or ICC criteria with KMT2A translocation by local standard diagnostic testing by cytogenetics\u002Fkaryotype or FISH\n\nExclusion Criteria:\n\n* Isolated myeloid sarcoma (patients must have blood or marrow involvement with AML to enter study)\n* Active central nervous system (CNS) involvement by AML. Of note, patients are eligible if CNS leukemia is in remission at the time of study entry.\n* Pregnant or breastfeeding (NOTE: breast milk cannot be stored for future use while the mother is being treated on study).","ALL","18 Years","65 Years",{"count":70,"type":71},88,"ESTIMATED","INTERVENTIONAL",[74],"PHASE2","This study is testing a new treatment combination called RAVEN, which includes revumenib, azacitidine, and venetoclax, in patients who are newly diagnosed with a specific type of acute myeloid leukemia (AML) called KMT2A- translocated AML.\n\nPeople with this type of AML often have poor outcomes, so new treatments are needed that may work better and cause fewer side effects.\n\nThe study has two parts:\n\n1. Induction Phase: Patients will receive treatment for up to 3 cycles. Each cycle lasts 28 days. The goal is to help the leukemia go into remission.\n2. Continuation Phase: After remission and blood count recovery, patients will continue treatment until the leukemia returns, side effects become too severe, the patient receives a stem cell transplant, or another reason to stop treatment occurs.\n\nPatients who receive an allogeneic stem cell transplant (stem cells from a donor) may also join a separate part of the study to test revumenib as maintenance treatment after transplant.",[77],"Leukemia Acute Myeloid",[79,80,81,82],"revumenib","azacitidine","venetoclax","allogeneic stem cell transplant","NOT_YET_RECRUITING","2026-06-26",{"date":86,"type":87},"2026-06-30","ACTUAL",{"date":89,"type":71},"2026-07",{"date":91,"type":71},"2028-07",{"name":5,"class":6},1]