Drug intelligence / Profile preview

azacitidine or decitabine

Development stage
Unknown
Lead developer
Bristol Myers Squibb
Modality
Small Molecules
Administration
Intravenous, Subcutaneous
01

Overview

Azacitidine or decitabine refers to the use of either azacitidine or decitabine, two closely related hypomethylating agents, as alternative options for the treatment of hematologic malignancies. Both drugs are nucleoside analogs that inhibit DNA methyltransferases, leading to DNA hypomethylation and reactivation of silenced tumor suppressor genes. Azacitidine is primarily incorporated into RNA (with some incorporation into DNA), while decitabine is incorporated only into DNA. Both drugs are approved for myelodysplastic syndromes (MDS) and are also used in acute myeloid leukemia (AML), especially in patients who are elderly or unfit for intensive chemotherapy[1][3][5][9]. They have similar mechanisms but differ slightly in their pharmacology and clinical profiles.

02

Targets

DNMT3A (DNA methyltransferase 3 alpha)DNMT3B (DNA (cytosine-5)-methyltransferase 3B)DNMT1 (DNA (cytosine-5)-methyltransferase 1)

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