Drug intelligence / Profile preview

emavusertib + azacitidine + venetoclax

Development stage
Unknown
Lead developer
Curis
Modality
Small Molecules
Administration
Intravenous, Oral, Subcutaneous
01

Overview

Emavusertib + azacitidine + venetoclax is an investigational triple-drug combination regimen being developed by Curis for the treatment of acute myeloid leukemia (AML). The regimen combines emavusertib (CA-4948), an oral small-molecule inhibitor of interleukin-1 receptor-associated kinase 4 (IRAK4) and FMS-like tyrosine kinase 3 (FLT3), with the standard-of-care backbone of azacitidine (a hypomethylating agent) and venetoclax (a BCL-2 inhibitor). This triplet therapy is designed to target multiple survival pathways in leukemia cells and overcome resistance mechanisms, such as FLT3 mutations or MCL-1 upregulation, which often lead to relapse on the doublet of azacitidine and venetoclax. It is currently being evaluated in clinical trials, including the Phase 1 TakeAim Leukemia study (CA-4948-104), as an add-on therapy to achieve undetectable measurable residual disease (uMRD) in AML patients who are in complete response but remain MRD-positive.

Other names
CA-4948 + azacitidine + venetoclaxema + ven + azaema-ven-azaemavusertib + venetoclax + azacitidineemavusertib, azacitidine, and venetoclaxemavusertib, venetoclax, and azacitidine
02

Targets

BCL-2 (BCL-2 family)CLK1 (CDC-like kinase 1)CLK2 (CDC-like kinase 2)CLK4DNMT1 (DNA (cytosine-5)-methyltransferase 1)FLT3 (Fms related receptor tyrosine kinase 3)IRAK4 (Interleukin-1 receptor associated kinase 4)

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