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AC220

Known as: AC-220, AC010220 
National Institutes of Health

Papers overview

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Highly Cited
2015
Highly Cited
2015
In acute myeloid leukemia (AML), about 25–30% of patients harbor a constitutively active receptor tyrosine kinase (RTK) FLT3… 
2014
2014
The vast majority of acute myeloid leukemia (AML) patients harboring an FLT3-ITD mutation experience relapse within a short… 
2014
2014
7100 Background: The presence of FLT3-internal tandem duplication (ITD) in patients (pts) with acute myeloid leukemia (AML) is… 
Highly Cited
2013
Highly Cited
2013
Secondary point mutations in the Fms-like tyrosine kinase 3 (FLT3) tyrosine kinase domain (KD) are common causes of acquired… 
2013
2013
Introduction AC220 (Quizartinib) is a novel FLT3 inhibitor that has shown a high level of activity as monotherapy in patients… 
2013
2013
FMS-like tyrosine kinase 3 internal tandem duplications (FLT3-ITD) in acute myeloid leukemia (AML) are associated with early… 
Review
2012
Review
2012
The treatment of acute myeloid leukemia has not changed significantly over the last 40 years. Recent progress in understanding… 
Highly Cited
2009
Highly Cited
2009
Abstract 636 Activating mutations in the FLT3 RTK are present in ∼30% of AML patients (pts), who have a significantly worse…