[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100338206":3},{"organization":4,"armGroups":7,"interventions":15,"overallOfficials":43,"centralContacts":47,"locations":53,"responsibleParty":71,"collaborators":73,"id":77,"slug":78,"hasResults":79,"nctId":80,"briefTitle":81,"officialTitle":82,"acronym":51,"eligibilityCriteria":83,"healthyVolunteers":79,"sex":84,"minAge":85,"maxAge":51,"enrollmentInfo":86,"targetDuration":51,"studyType":89,"phases":90,"briefSummary":92,"conditions":93,"keywords":51,"overallStatus":56,"whyStopped":51,"lastUpdateSubmitDate":101,"lastUpdatePostDateStruct":102,"startDateStruct":105,"completionDateStruct":107,"leadSponsor":109,"locationsCount":110},{"fullName":5,"class":6},"M.D. Anderson Cancer Center","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Treatment (azacitidine, enasidenib mesylate)","EXPERIMENTAL","Patients receive azacitidine SC or IV over 30 minutes on days 1-7 and enasidenib mesylate PO QD beginning on day 1. Cycles repeat every 4-6 weeks in the absence of disease progression or unacceptable toxicity.",[13,14],"Drug: Azacitidine","Drug: Enasidenib Mesylate",[16,32],{"type":17,"name":18,"description":19,"armGroupLabels":20,"otherNames":21},"DRUG","Azacitidine","Given SC or IV",[9],[22,23,24,25,26,27,28,29,30,31],"5 AZC","5-AC","5-Azacytidine","5-AZC","Azacytidine","Azacytidine, 5-","Ladakamycin","Mylosar","U-18496","Vidaza",{"type":17,"name":33,"description":34,"armGroupLabels":35,"otherNames":36},"Enasidenib Mesylate","Given PO",[9],[37,38,39,40,41,42],"2-Methyl-1-[(4-[6-(trifluoromethyl)pyridin-2-yl]-6-{[2-(trifluoromethyl)pyridin-4-yl]amino}-1,3,5-triazin-2-yl)amino]propan-2-ol Methanesulfonate","2-Propanol, 2-Methyl-1-((4-(6-(trifluoromethyl)-2-pyridinyl)-6-((2-(trifluoromethyl)-4-pyridinyl)amino)-1,3,5-triazin-2-yl)amino)-, Methanesulfonate (1:1)","AG-221 Mesylate","CC-90007","Enasidenib Methanesulfonate","Idhifa",[44],{"name":45,"affiliation":5,"role":46},"Courtney DiNardo","PRINCIPAL_INVESTIGATOR",[48],{"name":45,"role":49,"phone":50,"phoneExt":51,"email":52},"CONTACT","713-794-1141",null,"cdinardo@mdanderson.org",[54],{"facility":55,"status":56,"city":57,"state":58,"zip":59,"country":60,"countryCode":61,"cosmosGeoPoint":62,"geoPoint":67,"contacts":68},"M D Anderson Cancer Center","RECRUITING","Houston","Texas","77030","United States","US",{"type":63,"coordinates":64},"Point",[65,66],-95.36327,29.76328,{"lat":66,"lon":65},[69,70],{"name":45,"role":49,"phone":50,"phoneExt":51,"email":51},{"name":45,"role":46,"phone":51,"phoneExt":51,"email":51},{"type":72,"investigatorFullName":51,"investigatorTitle":51,"investigatorAffiliation":51,"oldNameTitle":51,"oldOrganization":51},"SPONSOR",[74],{"name":75,"class":76},"National Cancer Institute (NCI)","NIH","100338206","phase-2-enasidenib-and-azacitidine-in-treating-patients-with-recurrent-or-refractory-acute-myeloid-leukemia-and-idh2-gene-mutation-100338206",false,"NCT03683433","Enasidenib and Azacitidine in Treating Patients With Recurrent or Refractory Acute Myeloid Leukemia and IDH2 Gene Mutation","Phase II Study of the Targeted Mutant IDH2 Inhibitor Enasidenib in Combination With Azacitidine for Relapsed\u002FRefractory AML","Inclusion Criteria:\n\n* Patients with AML or biphenotypic or bilineage leukemia (including a myeloid component) who have failed prior therapy. Patients with isolated extramedullary AML are eligible. The World Health Organization (WHO) classification will be used for AML\n* Elderly (\\> 60 years old) patients with newly diagnosed AML not eligible for intensive chemotherapy are also eligible\n* AML patients with prior history of myelodysplastic syndrome (MDS) or chronic myelomonocytic leukemia (CMML) regardless of prior therapy received, are eligible at the time of diagnosis of AML\n* Subjects must have documented IDH2 gene mutation\n* Eastern Cooperative Oncology Group (ECOG) performance status =\\\u003C 3\n* Adequate renal function including creatinine \\\u003C 2 unless related to the disease\n* Total bilirubin \\\u003C 2 x upper limit of normal (ULN) unless increase is due to Gilbert's disease or leukemic involvement\n* Aspartate aminotransferase (AST) and\u002For alanine aminotransferase (ALT) \\\u003C 3 x ULN unless considered due to leukemic involvement\n* Provision of written informed consent\n* Oral hydroxyurea and\u002For cytarabine (up to 2 g\u002Fm2) for patients with rapidly proliferative disease is allowed before the start of study therapy, as needed, for clinical benefit and after discussion with the principal investigator (PI). Concurrent therapy for central nervous system (CNS) prophylaxis or continuation of therapy for controlled CNS disease is permitted\n* Females must be surgically or biologically sterile or postmenopausal (amenorrheic for at least 12 months) or if of childbearing potential, must have a negative serum or urine pregnancy test within 72 hours before the start of the treatment\n* Women of childbearing potential must agree to use an adequate method of contraception during the study and until 3 months after the last treatment. Males must be surgically or biologically sterile or agree to use an adequate method of contraception during the study until 3 months after the last treatment\n\nExclusion Criteria:\n\n* Patients with t(15;17) karyotypic abnormality or acute promyelocytic leukemia (French-American-British \\[FAB\\] class M3-AML)\n* Active and uncontrolled comorbidities including active uncontrolled infection, uncontrolled hypertension despite adequate medical therapy, active and uncontrolled congestive heart failure New York Heart Association (NYHA) class III\u002FIV, clinically significant and uncontrolled arrhythmia as judged by the treating physician\n* Any other medical, psychological, or social condition that may interfere with study participation or compliance, or compromise patient safety in the opinion of the investigator\n* Pregnant or breastfeeding","ALL","18 Years",{"count":87,"type":88},50,"ESTIMATED","INTERVENTIONAL",[91],"PHASE2","This phase II trial studies how well enasidenib and azacitidine work in treating patients with IDH2 gene mutation and acute myeloid leukemia that has come back (recurrent) or does not respond to treatment (refractory). Enasidenib and azacitidine may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth.",[94,95,96,97,98,99,100],"Acute Bilineal Leukemia","Acute Biphenotypic Leukemia","Chronic Myelomonocytic Leukemia","IDH2 Gene Mutation","Myelodysplastic Syndrome","Recurrent Acute Myeloid Leukemia","Refractory Acute Myeloid Leukemia","2026-03-03",{"date":103,"type":104},"2026-03-05","ACTUAL",{"date":106,"type":104},"2018-09-18",{"date":108,"type":88},"2027-09-20",{"name":5,"class":6},1]