Drug intelligence / Profile preview

irinotecan liposome + capecitabine + lenvatinib

Development stage
Unknown
Lead developer
Jiangsu HengRui Medicine Co., Ltd.
Modality
Small Molecules, Nanoparticles → Drug Delivery Systems
Administration
Intravenous, Oral
01

Overview

This drug combination is a multi-modality therapeutic regimen being evaluated for the second-line treatment of advanced or metastatic biliary tract carcinoma (BTC). It consists of **irinotecan liposome**, a nanoparticle formulation of the topoisomerase I inhibitor irinotecan designed for prolonged systemic exposure and enhanced tumor accumulation; **capecitabine**, an oral fluoropyrimidine carbamate that functions as a cytotoxic prodrug of 5-fluorouracil; and **lenvatinib**, an oral multi-kinase inhibitor targeting VEGFR1-3, FGFR1-4, PDGFRα, KIT, and RET. The regimen, studied in clinical trials led by investigator Yunpeng Liu, aims to leverage the synergistic effects of cytotoxic chemotherapy and targeted anti-angiogenic therapy to overcome resistance in refractory biliary tract cancers.

Other names
Irinotecan hydrochloride liposome injection + Capecitabine + LenvatinibIrinotecan liposome plus Capecitabine and Lenvatinib
02

Targets

KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDGFRA (Platelet-derived growth factor receptor alpha)RET (Rearranged during transfection receptor tyrosine kinase)TS (Thymidylate synthase)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)TOP1 (DNA Topoisomerase I)FGFR1 (Fibroblast growth factor receptor 1)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)

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