Drug intelligence / Profile preview

anlotinib + carboplatin + paclitaxel

Development stage
Unknown
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Small Molecules
Administration
Oral (anlotinib), Intravenous (carboplatin, Paclitaxel)
01

Overview

This is a combination drug regimen consisting of **anlotinib**, **carboplatin**, and **paclitaxel**, used investigationally as a first-line or second-line therapy for certain advanced cancers, notably non-small cell lung cancer (NSCLC) and ovarian cancer. - **Anlotinib** is a small molecule multi-target receptor tyrosine kinase (RTK) inhibitor with anti-angiogenic and anti-tumor properties. It targets vascular endothelial growth factor receptors (VEGFR1/2/3), fibroblast growth factor receptors (FGFR1/2/3/4), platelet-derived growth factor receptors (PDGFRα/β), and c-Kit, thereby inhibiting angiogenesis and tumor cell proliferation. - **Carboplatin** is a platinum-based chemotherapeutic agent that forms DNA cross-links, resulting in apoptosis of rapidly dividing tumor cells. - **Paclitaxel** is a microtubule-stabilizing agent that disrupts cell division and induces apoptosis by binding to tubulin. This combination, including maintenance therapy with anlotinib, is mainly being studied for efficacy and safety in patients with advanced or metastatic NSCLC (particularly EGFR/ALK wild-type non-squamous NSCLC) and advanced ovarian cancer, showing improved progression-free and overall survival versus historical chemotherapy controls[3][4][5].

Brand names
CatequentinibTaxolParaplatin
Other names
AL3818AL-3818AL 3818Catequentinib
02

Targets

VEGFR2 (Vascular endothelial growth factor receptor 2)DNAVEGFR3 (Vascular endothelial growth factor receptor 3)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR (FGFR family)

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