[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100570457":3},{"organization":4,"armGroups":7,"interventions":20,"overallOfficials":32,"centralContacts":36,"locations":41,"responsibleParty":135,"collaborators":138,"id":142,"slug":143,"hasResults":144,"nctId":145,"briefTitle":146,"officialTitle":147,"acronym":31,"eligibilityCriteria":148,"healthyVolunteers":144,"sex":149,"minAge":150,"maxAge":151,"enrollmentInfo":152,"targetDuration":31,"studyType":155,"phases":156,"briefSummary":158,"conditions":159,"keywords":163,"overallStatus":44,"whyStopped":31,"lastUpdateSubmitDate":166,"lastUpdatePostDateStruct":167,"startDateStruct":170,"completionDateStruct":172,"leadSponsor":174,"locationsCount":175},{"fullName":5,"class":6},"Massachusetts General Hospital","OTHER",[8,14],{"label":9,"type":10,"description":11,"interventionNames":12},"Ivosidenib","EXPERIMENTAL","After screening and standard of care hematopoietic stem cell transplantation (HCT) and any standard treatment before and after the HSCT, Ivosidenib will be given orally (PO) once daily (QD) in 28-day continuous cycles. Ivosidenib is administered at a pre-determined dose with a goal of 500mg daily. Participants begin study treatment 45 to 90 days after HCT, and treatment will continue for up to 24 months. Study visits and assessments occur throughout study treatment and in follow-up. After the 24-month treatment period, participants are followed for up to 12 additional months.",[13],"Drug: Ivosidenib",{"label":15,"type":16,"description":17,"interventionNames":18},"Placebo","PLACEBO_COMPARATOR","After screening and standard of care hematopoietic stem cell transplantation (HCT) and any standard treatment before and after the HSCT, Placebo will be given orally (PO) once daily (QD) in 28-day continuous cycles. Participants begin study treatment (placebo) 45 to 90 days after HCT, and treatment (placebo) will continue for up to 24 months. Study visits and assessments occur throughout study treatment period and in follow-up. After the 24-month treatment period, participants are followed for up to 12 additional months.",[19],"Drug: Placebo",[21,28],{"type":22,"name":9,"description":23,"armGroupLabels":24,"otherNames":25},"DRUG","Ivosidenib tablets are supplied as 50 mg, 200 mg, and 250 mg strengths, to be taken orally.",[9],[26,27],"AG-120","S95031",{"type":22,"name":15,"description":29,"armGroupLabels":30,"otherNames":31},"Placebo tablets are taken orally.",[15],null,[33],{"name":34,"affiliation":5,"role":35},"Amir T Fathi, MD","PRINCIPAL_INVESTIGATOR",[37],{"name":34,"role":38,"phone":39,"phoneExt":31,"email":40},"CONTACT","617-724-1124","afathi@mgh.harvard.edu",[42,62,75,87,103,119],{"facility":43,"status":44,"city":45,"state":46,"zip":47,"country":48,"countryCode":49,"cosmosGeoPoint":50,"geoPoint":55,"contacts":56},"Emory University Hospital","RECRUITING","Atlanta","Georgia","30322","United States","US",{"type":51,"coordinates":52},"Point",[53,54],-84.38798,33.749,{"lat":54,"lon":53},[57,61],{"name":58,"role":38,"phone":59,"phoneExt":31,"email":60},"Amelia Langston, MD","404-778-0519","alangst@emory.edu",{"name":58,"role":35,"phone":31,"phoneExt":31,"email":31},{"facility":5,"status":44,"city":63,"state":64,"zip":65,"country":48,"countryCode":49,"cosmosGeoPoint":66,"geoPoint":70,"contacts":71},"Boston","Massachusetts","02114",{"type":51,"coordinates":67},[68,69],-71.05977,42.35843,{"lat":69,"lon":68},[72,73],{"name":34,"role":38,"phone":39,"phoneExt":31,"email":40},{"name":74,"role":35,"phone":31,"phoneExt":31,"email":31},"Amir Fathi, MD",{"facility":76,"status":44,"city":63,"state":64,"zip":77,"country":48,"countryCode":49,"cosmosGeoPoint":78,"geoPoint":80,"contacts":81},"Dana Farber Cancer Institute","02115",{"type":51,"coordinates":79},[68,69],{"lat":69,"lon":68},[82,86],{"name":83,"role":38,"phone":84,"phoneExt":31,"email":85},"Robert Soiffer, MD","617-632-4731","Robert_Soiffer@dfci.harvard.edu",{"name":83,"role":35,"phone":31,"phoneExt":31,"email":31},{"facility":88,"status":44,"city":89,"state":90,"zip":91,"country":48,"countryCode":49,"cosmosGeoPoint":92,"geoPoint":96,"contacts":97},"Ohio State University Wexner Medical Center- James Cancer Hospital","Columbus","Ohio","43210",{"type":51,"coordinates":93},[94,95],-82.99879,39.96118,{"lat":95,"lon":94},[98,102],{"name":99,"role":38,"phone":100,"phoneExt":31,"email":101},"Jiasheng Wang, MD","614-293-3196","jiasheng.wang@osumc.edu",{"name":99,"role":35,"phone":31,"phoneExt":31,"email":31},{"facility":104,"status":44,"city":105,"state":106,"zip":107,"country":48,"countryCode":49,"cosmosGeoPoint":108,"geoPoint":112,"contacts":113},"Huntsman Cancer Institute, University of Utah","Salt Lake City","Utah","84112",{"type":51,"coordinates":109},[110,111],-111.89105,40.76078,{"lat":111,"lon":110},[114,118],{"name":115,"role":38,"phone":116,"phoneExt":31,"email":117},"Sagar Patel, MD","801-587-9014","Sagar.Patel@hci.utah.edu",{"name":115,"role":35,"phone":31,"phoneExt":31,"email":31},{"facility":120,"status":44,"city":121,"state":122,"zip":123,"country":48,"countryCode":49,"cosmosGeoPoint":124,"geoPoint":128,"contacts":129},"Froedtert Hospital & the Medical College of Wisconsin","Milwaukee","Wisconsin","53226",{"type":51,"coordinates":125},[126,127],-87.90647,43.0389,{"lat":127,"lon":126},[130,134],{"name":131,"role":38,"phone":132,"phoneExt":31,"email":133},"Sameem Abedin, MD","414-805-4600","sabedin@mcw.edu",{"name":131,"role":35,"phone":31,"phoneExt":31,"email":31},{"type":35,"investigatorFullName":136,"investigatorTitle":137,"investigatorAffiliation":5,"oldNameTitle":31,"oldOrganization":31},"Amir Fathi","Principal Investigator",[139],{"name":140,"class":141},"Servier","INDUSTRY","100570457","phase-2-ivosidenib-as-post-hsct-maintenance-for-aml-100570457",false,"NCT06707493","Ivosidenib as Post-HSCT Maintenance for AML","A Randomized, Placebo-Controlled Phase 2 Study of IDH1 Inhibition Using Ivosidenib as Maintenance Therapy for IDH1-mutant Acute Myeloid Leukemia Following Allogeneic Stem Cell Transplantation","Inclusion Criteria:\n\n* Pathologically confirmed diagnosis of IDH1(R132)-mutant acute myeloid leukemia (AML). IDH1 mutations could have been detected by any mutational technique at any prior point including at diagnosis or remission.\n* Between the ages of 18 and 75 years\n* Will undergo allogeneic hematopoietic stem cell transplantation (HSCT) for their malignancy. Conditioning may be either conventional myeloablative (MAC) or reduced intensity conditioning (RIC). There will be no restrictions on type of graft source.\n* ECOG performance status ≤ 2\n* Participants must have normal organ and marrow function as defined below:\n\n  * Absolute neutrophil count ≥ 1000\u002FµL without growth factor support (e.g. GCSF) in the previous 7 days.\n  * Platelet count ≥ 50,000\u002FµL without transfusional support in the previous 7 days.\n  * AST (SGOT), ALT (SGPT) and Alkaline phosphatase \\\u003C 3x institutional upper limit of normal (ULN)\n  * Direct bilirubin \\\u003C 2.0 mg\u002FdL\n  * Calculated creatinine clearance ≥ 40 mL\u002Fmin (Cockcroft-Gault formula)\n* LVEF must be equal to or greater than 40%, as measured by MUGA scan or echocardiogram\n* Female patients of childbearing potential must have a negative pregnancy test\n* The effects of ivosidenib on the developing human fetus are unknown. For this reason female participants of child-bearing potential and male participants must agree to use adequate contraception (hormonal or barrier method of birth control; abstinence) during the entire study treatment period and through 90 days after the last dose of treatment\n* Ability to understand and the willingness to sign a written informed consent document.\n\nExclusion Criteria:\n\n* Prior allogeneic hematopoietic stem cell transplants.\n* Morphologically relapsed or refractory disease, as assessed by bone marrow aspirate and biopsy performed within 42 days prior to study entry\n* History of other malignancy(ies) unless\n\n  * the participant has been disease-free for at least 5 years and is deemed by the investigator to be at low risk of recurrence of that malignancy, or\n  * the only prior malignancy was cervical cancer in situ and\u002For basal cell or squamous cell carcinoma of the skin\n* Known diagnosis of active hepatitis B or hepatitis C\n* Current or history of congestive heart failure New York Heart Association (NHYA) class 3 or 4, or any history of documented diastolic or systolic dysfunction (LVEF \\\u003C 40%, as measured by MUGA scan or echocardiogram)\n* Current or history of ventricular or life-threatening arrhythmias or diagnosis of long-QT syndrome\n* QTc interval (i.e., Friderica's correction \\[QTcF\\]) ≥ 450 ms or other factors that increase the risk of QT prolongation or arrhythmic events (e.g., heart failure, hypokalemia, family history of long QT interval syndrome) at screening\n* Uncontrolled intercurrent illness that would limit compliance with study requirements.\n\nPost-transplantation Pre-Treatment Criteria Treatment may begin at any time between day 45 and day 90 following stem cell transplantation.\n\nHowever, at time of treatment start, it must be ensured that:\n\n* The patient has continued willingness and interest in participating in the study.\n* There is no systemic infection requiring IV antibiotic therapy within 7 days preceding the first dose of study drug, or other severe infection\n* Chimerism studies reveal that ≥ 70% of blood or bone marrow cells, or of the CD33 expressing fraction, are of donor origin,\n* There is no acute graft versus host disease (GVHD), requiring an equivalent dose of ≥ 0.5mg\u002Fkg\u002Fday of prednisone within one week of starting ivosidenib \u002F placebo, or have escalation of systemic immunosuppression in terms of increase of corticosteroids or addition of new agent\u002Fmodality within two weeks of starting ivosidenib \u002F placebo.\n* For prophylaxis for GVHD, agents that are permitted for administration on study:\n\n  * Tacrolimus\n  * Cyclosporine\n  * Sirolimus\n  * Cyclophosphamide\n  * Mycophenolate Mofetil\n  * Methotrexate\n  * ATG\n  * Ruxolitinib\n  * Vedolizumab\n  * As standards of care may change, any other prophylactic agents used should be discussed with the PI.\n* Investigational agents, defined as not approved for any indication, are forbidden unless the participant comes off study.\n\n  * Agents used to treat GVHD that are permitted for administration on study:\n  * Any agent used in prophylaxis may be continued (see list above)\n\n    * Ruxolitinib\n    * Etanarcept\n    * ATG\n    * Belumosidil\n    * Axatilimab\n    * Rituximab\n    * Fecal microbiota transplantation\n    * Alpha1-Antitrypsin\n    * Pregnyl\n    * Extracorporal photopheresis (ECP)\n  * As standards of care may change, any other treatment agents used should be discussed with the PI.\n  * Investigational agents, defined as not approved for any indication, are forbidden unless the participant comes off study.\n* There is no evidence of relapsed\u002Frecurrent\u002Fresidual disease.\n* Prior to the start of ivosidenib \u002F placebo administration, the participant must have adequate hematological function, defined as:\n\n  * ANC ≥ 1000\u002FµL\n  * Platelets ≥ 50,000\u002FµL\n\nand adequate organ function defined as\n\n* Direct bilirubin level \\\u003C 2.0 mg\u002FdL\n* AST (SGOT), ALT (SGPT) and Alkaline phosphatase \\\u003C 3x institutional upper limit of normal (ULN)\n* No presence of congestive heart failure, defined by New York Heart Association (NHYA) criteria as class 3 or 4\n* Calculated creatinine clearance ≥ 40 mL\u002Fmin (Cockcroft-Gault formula)","ALL","18 Years","75 Years",{"count":153,"type":154},75,"ESTIMATED","INTERVENTIONAL",[157],"PHASE2","This is a Phase 2 study of the study drug, ivosidenib (a mutant IDH1 inhibitor), compared to placebo, given to patients with IDH1-mutant acute myeloid leukemia (AML) after hematopoietic stem cell transplantation (HCT).",[160,161,162],"IDH1 Mutation","Acute Myeloid Leukemia (AML)","Hematopoietic Stem Cell Transplant (HSCT)",[164,165],"hematopoietic stem cell transplantation (HCT)","IDH1-mutant acute myeloid leukemia (AML)","2026-06-17",{"date":168,"type":169},"2026-06-18","ACTUAL",{"date":171,"type":169},"2026-01-16",{"date":173,"type":154},"2030-01-01",{"name":5,"class":6},6]