Drug intelligence / Profile preview

anlotinib hydrochloride + irinotecan + docetaxel

Development stage
Unknown
Lead developer
Hangzhou First People's Hospital
Modality
Small Molecules
Administration
Oral, Intravenous
01

Overview

This is an investigational combination chemotherapy and targeted therapy regimen being evaluated for the second-line treatment of extensive-stage small-cell lung cancer (ES-SCLC). The regimen consists of anlotinib hydrochloride, a multi-target tyrosine kinase inhibitor (TKI) that inhibits vascular endothelial growth factor receptor (VEGFR), fibroblast growth factor receptor (FGFR), platelet-derived growth factor receptor (PDGFR), and c-Kit; irinotecan, a topoisomerase I inhibitor; and docetaxel, a taxane that stabilizes microtubules. This specific combination is being studied in a Phase 2 clinical trial (NCT04757779) sponsored by the First People's Hospital of Hangzhou for patients who have relapsed after first-line platinum-based chemotherapy. In the trial, anlotinib is administered orally, while irinotecan or docetaxel are administered intravenously as separate treatment arms.

Other names
anlotinib + irinotecan + docetaxelanlotinib hydrochloride combined with irinotecan or docetaxelAL3818 + CPT-11 + docetaxel
02

Targets

TUBB (Tubulin (alpha and beta subunits))VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRA (Platelet-derived growth factor receptor alpha)VEGFR-1 (Vascular endothelial growth factor receptor 1)TOP1 (DNA Topoisomerase I)VEGFR3 (Vascular endothelial growth factor receptor 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR (FGFR family)RET (Rearranged during transfection receptor tyrosine kinase)

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