Drug intelligence / Profile preview

benmelstobart + anlotinib + etoposide

Development stage
Phase 3
Lead developer
Chia Tai-Tianqing Pharmaceutical Group
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

Benmelstobart + anlotinib + etoposide is a combination therapeutic regimen primarily used as a first-line treatment for extensive-stage small cell lung cancer (ES-SCLC). The regimen consists of **benmelstobart**, a humanized IgG1 monoclonal antibody that acts as a programmed death-ligand 1 (PD-L1) inhibitor; **anlotinib**, a multi-target small molecule tyrosine kinase inhibitor that targets vascular endothelial growth factor receptors (VEGFR 1-3), fibroblast growth factor receptors (FGFR 1-4), platelet-derived growth factor receptors (PDGFR α/β), and c-Kit; and **etoposide**, a standard cytotoxic chemotherapy agent that inhibits DNA topoisomerase II. This triplet therapy was evaluated in the pivotal Phase 3 ETER701 trial, which demonstrated a significant improvement in both progression-free survival (PFS) and overall survival (OS) compared to standard chemotherapy. Benmelstobart was developed by Chia Tai Tianqing Pharmaceutical Group and received approval from China's NMPA in May 2024 for use in this combination for first-line SCLC.

Other names
benmelstobart combined with anlotinib and etoposide
02

Targets

TOP2A (DNA topoisomerase II)FGFR (FGFR family)CD274 (Programmed cell death protein 1 ligand 1)PDGFRA (Platelet-derived growth factor receptor alpha)RET (Rearranged during transfection receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)

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