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Accordingly, data for other dose levels(100mg QD, 150mg QD, and 300mg QD) were combined as prespecified in SAP.","eventGroups":[{"deathsNumAffected":4,"deathsNumAtRisk":16,"description":"Participants with AML or MDS received single agent FT-2102 orally BID in 28-day cycles at dose levels of 150 mg until MTD or MED achieved.","id":"EG000","otherNumAffected":15,"otherNumAtRisk":16,"seriousNumAffected":10,"seriousNumAtRisk":16,"title":"Phase 1: FT-2102 (Single Agent)"},{"deathsNumAffected":11,"deathsNumAtRisk":31,"description":"Participants with AML or MDS received single agent FT-2102 orally QD and BID in 28-day cycles at the different dose levels (150 mg and ≤ 300 mg) until MTD or MED achieved.","id":"EG001","otherNumAffected":29,"otherNumAtRisk":31,"seriousNumAffected":23,"seriousNumAtRisk":31,"title":"Phase 1: Total FT-2102 (Single Agent)"},{"deathsNumAffected":9,"deathsNumAtRisk":39,"description":"Participants with AML or MDS received combination therapy (FT-2102 + azacitidine 75 mg/m\\^2) orally BID in 28-day cycles at dose levels of 150 mg until MTD or MED achieved.","id":"EG002","otherNumAffected":39,"otherNumAtRisk":39,"seriousNumAffected":30,"seriousNumAtRisk":39,"title":"Phase 1: FT-2102 + Azacitidine (Combination Therapy)"},{"deathsNumAffected":10,"deathsNumAtRisk":46,"description":"Participants with AML or MDS received combination therapy (FT-2102 150 mg and ≤ 300 mg and azacitidine administered at the dose of 75 mg/m\\^2 for 7 days IV/SC per every 28-day cycle) until treatment discontinuation.","id":"EG003","otherNumAffected":46,"otherNumAtRisk":46,"seriousNumAffected":36,"seriousNumAtRisk":46,"title":"Phase 1: Total FT-2102; FT-2102 + Azacitidine (Combination Therapy)"},{"deathsNumAffected":21,"deathsNumAtRisk":78,"description":"Participants with AML or MDS received single agent (FT-2102), combination therapy (FT-2102 + azacitidine, FT-2102+ LDAC) starting at 150 mg BID dose level until MTD or MED achieved or treatment discontinuation.","id":"EG004","otherNumAffected":76,"otherNumAtRisk":78,"seriousNumAffected":60,"seriousNumAtRisk":78,"title":"Phase 1: Overall"},{"deathsNumAffected":50,"deathsNumAtRisk":153,"description":"Participants with R/R AML received single agent of FT-2102 150 mg BID in continuous 28-day cycles.","id":"EG005","otherNumAffected":152,"otherNumAtRisk":153,"seriousNumAffected":115,"seriousNumAtRisk":153,"title":"Phase 2: Cohort 1; FT-2102 (Single Agent)"},{"deathsNumAffected":0,"deathsNumAtRisk":18,"description":"Participants with AML in morphologic CR/CRi after prior therapy with residual IDH1-R132 mutation were received single agent of FT-2102 150 mg BID in continuous 28-day cycles.","id":"EG006","otherNumAffected":18,"otherNumAtRisk":18,"seriousNumAffected":6,"seriousNumAtRisk":18,"title":"Phase 2: Cohort 2; FT-2102 (Single Agent)"},{"deathsNumAffected":2,"deathsNumAtRisk":5,"description":"Participants with R/R AML or MDS who were previously treated with FT-2102 and who underwent HSCT on-study then relapsed post-HSCT received single agent of FT-2102 150 mg BID in continuous 28-day cycles.","id":"EG007","otherNumAffected":5,"otherNumAtRisk":5,"seriousNumAffected":4,"seriousNumAtRisk":5,"title":"Phase 2: Cohort 3; FT-2102 (Single Agent)"},{"deathsNumAffected":3,"deathsNumAtRisk":20,"description":"Participants with R/R AML that is naïve to prior hypomethylating therapy and IDH1 inhibitor therapy received combination therapy of azacitidine 75 mg/m\\^2 + FT-2102 150 mg BID in continuous 28-day cycles.","id":"EG008","otherNumAffected":18,"otherNumAtRisk":20,"seriousNumAffected":12,"seriousNumAtRisk":20,"title":"Phase 2: Cohort 4; FT-2102 + Azacitidine (Combination Therapy)"},{"deathsNumAffected":6,"deathsNumAtRisk":21,"description":"Participants with R/R AML/MDS that have inadequately responded to or have progressed on prior hypo-methylating therapy received combination therapy of azacitidine 75 mg/m\\^2 + FT-2102 150 mg BID in continuous 28-day cycles.","id":"EG009","otherNumAffected":20,"otherNumAtRisk":21,"seriousNumAffected":18,"seriousNumAtRisk":21,"title":"Phase 2: Cohort 5; FT-2102 + Azacitidine (Combination Therapy)"},{"deathsNumAffected":7,"deathsNumAtRisk":20,"description":"Participants with R/R AML/MDS that have been previously treated with single agent FT-2102 as their last therapy prior to study enrolment received combination therapy of azacitidine + FT-2102 150 mg BID in continuous 28-day cycles. 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