Drug intelligence / Profile preview

ABT-869 + paclitaxel

Development stage
Unknown
Lead developer
AbbVie
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

ABT-869 (linifanib) + paclitaxel is an investigational combination therapy evaluated primarily in oncology, especially breast carcinoma and non-small cell lung cancer (NSCLC). ABT-869 (linifanib) is a selective, orally bioavailable **receptor tyrosine kinase (RTK) inhibitor** targeting vascular endothelial growth factor (VEGF) and platelet-derived growth factor (PDGF) receptor families, as well as mutant constitutively active FLT3 and KIT kinases. Its primary mechanism is antiangiogenic and antiproliferative action by inhibiting tumor cell signaling and vasculature. Paclitaxel is an established **microtubule inhibitor** that stabilizes microtubules, preventing cell division. Preclinical and phase 1/2 studies demonstrate that the combination enhances antitumor efficacy, particularly in breast and lung cancers, compared to either agent alone, with reported partial responses in metastatic breast cancer and tolerability concerns primarily related to the ABT-869 dose[1][2][3][5][6][7][8][9].

Other names
linifanib + paclitaxel
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)TUBB (Tubulin (alpha and beta subunits))PDGFRB (Platelet-derived growth factor receptor beta)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)CSF1R (Macrophage colony-stimulating factor receptor)FLT3 (Fms related receptor tyrosine kinase 3)

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