The purpose of this study is to learn more about the safety and efficacy of ivosidenib taken with azacitidine to treat adult patients with acute myeloid leukemia (AML) who are presenting a gene mutation called IDH1 (isocitrate dehydrogenase1 mutation-positive \[IDH1m\]) and cannot receive treatment with intensive chemotherapy (IC).
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Number of Adverse Events (AEs)
Timeframe: up to week 116
Number of Serious Adverse Events (SAEs)
Timeframe: up to week 116
Differentiation Syndrome of Grade 2 or higher
Timeframe: up to week 116
Number of Adverse Events (AEs) leading to ivosidenib + azacitidine discontinuation
Timeframe: up to week 112
Number of Adverse Events (AEs) leading to ivosidenib + azacitidine interruption
Timeframe: up to week 112
Number of Adverse Events (AEs) leading to ivosidenib + azacitidine dose reduction
Timeframe: up to week 112
Number of Adverse Events (AEs) leading to death
Timeframe: up to week 116
Number of clinical laboratory anomalies assessed as Adverse Events (AEs)
Timeframe: up to week 116
Servier Affaires Médicales
Number of patients requiring transfusion (platelet and RBC) and the average number of units transfused
Timeframe: up to week 116
Rate of infections
Timeframe: up to week 116
QT Prolongation event assessed as Grade 3 or higher
Timeframe: up to week 116