Drug intelligence / Profile preview

sunvozertinib + anlotinib

Development stage
Phase 2
Lead developer
Dizal Pharmaceutical
Modality
Small Molecules
Administration
Oral
01

Overview

Sunvozertinib + anlotinib is a combination therapy under investigation for the treatment of non-small cell lung cancer (NSCLC), particularly in patients with EGFR-sensitive mutations and co-mutations. Sunvozertinib is a small molecule inhibitor targeting the epidermal growth factor receptor (EGFR), including uncommon mutations such as exon 20 insertions. Anlotinib is a multi-targeted tyrosine kinase inhibitor that inhibits angiogenesis and tumor proliferation by targeting receptors such as VEGFR, FGFR, PDGFR, and c-Kit. The combination aims to provide synergistic antitumor activity by simultaneously blocking EGFR-driven tumor growth and angiogenesis pathways. This regimen is being evaluated primarily in advanced or metastatic NSCLC as first-line therapy for patients with specific genetic alterations[1][2][6][7].

Brand names
ShuwozheFukewei
Other names
third-generation EGFR-TKI + anlotinibsunvozertinib plus anlotinib
02

Targets

BTK (Bruton tyrosine kinase)HER2 exon 20 ins (Human epidermal growth factor receptor 2 (HER2) exon 20 insertion mutants)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)EGFR (Epidermal growth factor receptor)FGFR1 (Fibroblast growth factor receptor 1)PDGFRA (Platelet-derived growth factor receptor alpha)

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