Drug intelligence / Profile preview

decitabine + homoharringtonine + cytarabine + aclarubicin + G-CSF

Development stage
Phase 3
Lead developer
Eisai
Modality
Small Molecules, Recombinant Proteins and Enzymes
Administration
Intravenous, Subcutaneous
01

Overview

This is a five-drug combination chemotherapy regimen used primarily for the treatment of acute myeloid leukemia (AML), especially in elderly or high-risk patients. The regimen combines: - **Decitabine** (a hypomethylating agent that inhibits DNA methyltransferase, leading to reactivation of tumor suppressor genes and increased anti-tumor immunity) - **Homoharringtonine** (a plant alkaloid that inhibits protein synthesis and induces apoptosis in leukemia cells) - **Cytarabine** (an antimetabolite that inhibits DNA synthesis) - **Aclarubicin** (an anthracycline antibiotic with cytotoxic effects via intercalation into DNA and inhibition of topoisomerase II) - **G-CSF** (granulocyte colony-stimulating factor, which stimulates proliferation and differentiation of neutrophil precursors; used here as "priming" to enhance chemosensitivity) The combination is designed to maximize anti-leukemic efficacy by targeting multiple pathways involved in leukemogenesis while using G-CSF prim

Other names
HAAG regimenD-HAAGdecitabine plus HAAG
02

Targets

DNADNMT (DNA methyltransferase)DNA polymerase family80S A-site (Eukaryotic ribosomal aminoacyl-tRNA site (A-site))CSF3R (Granulocyte colony-stimulating factor receptor)TOP2A (DNA topoisomerase II)Neuraminidase

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