Drug intelligence / Profile preview

carboplatin + lenvatinib + paclitaxel

Development stage
Unknown
Lead developer
Eisai
Modality
DNA Intercalators/Alkylators → Nucleic Acid-Directed Small Molecules → Small Molecules
Administration
Intravenous, Oral
01

Overview

This is a combination regimen consisting of three drugs: - **Carboplatin**: a platinum-based chemotherapeutic agent that induces DNA crosslinking, leading to apoptosis in rapidly dividing cells. - **Lenvatinib**: an oral small molecule inhibitor targeting multiple receptor tyrosine kinases, including vascular endothelial growth factor receptors (VEGFR1–3), fibroblast growth factor receptors (FGFR1–4), platelet-derived growth factor receptor alpha (PDGFRα), RET, and KIT. It inhibits angiogenesis and tumor cell proliferation. - **Paclitaxel**: a microtubule-stabilizing agent that disrupts mitosis by promoting tubulin polymerization and inhibiting depolymerization. This combination has been studied primarily in advanced non-small-cell lung cancer (NSCLC) as well as being considered for gynecologic malignancies such as endometrial carcinoma. In phase 1 studies for NSCLC, the maximum tolerated dose of lenvatinib with carboplatin/paclitaxel was established at 4 mg twice daily[1][2]. The regimen demonstrated manageable tolerability and encouraging antitumor activity in early-phase trials[2].

02

Targets

FGFR4 (Fibroblast growth factor receptor 4)TUBB (Tubulin (alpha and beta subunits))PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)DNAFGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)FGFR2 (Keratinocyte growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)

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