Study Investigating the Efficacy of Crenolanib With Chemotherapy vs Chemotherapy Alone in R/R FLT3 Mutated AML

Inclusion Criteria:

Confirmed diagnosis of AML according to World Health Organization (WHO) 2016 classification
Presence of FLT3-ITD and/or D835 mutation(s)
Subjects must be primary refractory or relapsed to 1st line intensive treatment for AML or refractory or relapsed after second line of treatment for AML
Age ≥ 18 years and ≤ 75 years
Adequate hepatic function
Adequate renal functions
ECOG performance status ≤ 3

Exclusion Criteria:

Known clinically active central nervous system(CNS) leukemia
Severe liver disease
Known, active infection with hepatitis B virus (HBV) or hepatitis C virus (HCV)
Prior anti-leukemia therapy within the 14 days prior to randomization. Prior use of quizartinib or gilteritinib must be discontinued 21 days prior to randomization. Prior use of hydroxyurea or other palliative treatment for leukocytosis is allowed.
Previous treatment with crenolanib or prior participation in clinical trial involving crenolanib.