Drug intelligence / Profile preview

venetoclax + decitabine + azacytidine + cytarabine

Development stage
Unknown
Lead developer
The Fifth Medical Center of the PLA General Hospital
Modality
Small Molecules
Administration
Oral, Intravenous, Subcutaneous
01

Overview

This combination therapy is a triple-drug regimen being investigated by Beijing 302 Hospital for the treatment of relapsed/refractory acute myeloid leukemia (AML) or AML with positive minimal residual disease (MRD+). It consists of the BCL-2 inhibitor venetoclax, a hypomethylating agent (either decitabine or azacytidine), and low-dose cytarabine (LDAC). Venetoclax induces apoptosis in leukemia cells by inhibiting the anti-apoptotic protein BCL-2. Hypomethylating agents like decitabine and azacytidine work by inhibiting DNA methyltransferase, leading to DNA hypomethylation and reactivation of tumor suppressor genes. Cytarabine is a pyrimidine analog that interferes with DNA synthesis by inhibiting DNA polymerase. The combination aims to improve response rates in patients who have failed standard therapies.

Other names
Venetoclax + HMA + LDACVenetoclax + Hypomethylating Agent + Low-dose Cytarabine
02

Targets

DNMT1 (DNA (cytosine-5)-methyltransferase 1)BCL-2 (BCL-2 family)DNA

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