Drug intelligence / Profile preview

indoximod + idarubicin + cytarabine

Development stage
Unknown
Lead developer
Lumos Pharma
Modality
Small Molecules
Administration
Oral (indoximod), Intravenous (idarubicin), Intravenous (cytarabine)
01

Overview

This is a **three-drug combination regimen** consisting of **indoximod** (an oral small-molecule immunomodulator and tryptophan metabolism pathway inhibitor), **idarubicin** (an anthracycline antineoplastic agent), and **cytarabine** (a nucleoside analog antimetabolite). Indoximod inhibits the IDO (indoleamine 2,3-dioxygenase) pathway, which is associated with immune evasion by tumor cells. Idarubicin intercalates into DNA and inhibits topoisomerase II, leading to DNA strand breaks and apoptosis in rapidly dividing cells. Cytarabine is phosphorylated to its active form within leukemic cells and inhibits DNA synthesis by terminating DNA chain elongation. The three agents combined are studied primarily in **acute myeloid leukemia (AML)**, especially as part of **induction therapy** in newly diagnosed AML, for synergistic antitumor and immunomodulating effects[4][1][2][5][3]. Indoximod is an investigational drug, developed by NewLink Genetics, while idarubicin and cytarabine are widely used chemotherapeutic agents.

Other names
indoximod + idarubicin + cytarabine
02

Targets

DNA polymerase familyAHR (Aryl hydrocarbon receptor)DNAIDO1 (Indoleamine 2,3-dioxygenase 1)

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