Drug intelligence / Profile preview

omacetaxine + imatinib

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

Overview

**Omacetaxine + imatinib** is an experimental combination therapy investigated primarily for the treatment of chronic myeloid leukemia (CML), especially in advanced phases or cases resistant to tyrosine kinase inhibitors (TKIs). Omacetaxine mepesuccinate, a semisynthetic derivative of homoharringtonine, is a protein translation inhibitor that downregulates key oncoproteins including BCR-ABL. Imatinib is a small molecule tyrosine kinase inhibitor that targets the BCR-ABL fusion protein, the major driver oncogene in CML. The combination aims to provide synergistic inhibition of leukemic cells by attacking the disease via distinct mechanisms, showing preclinical and some clinical efficacy in TKI-resistant and advanced CML, with most studies conducted in academic and clinical trial settings.

02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)ABL1 (ABL proto-oncogene 1, non-receptor tyrosine kinase)dC (Deoxycytidine)

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