Drug intelligence / Profile preview

anlotinib + benmelstobart + cisplatin + gemcitabine

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

Overview

This combination therapy is a four-drug regimen being investigated for the treatment of advanced or metastatic urothelial carcinoma (bladder cancer). It consists of **anlotinib**, a multi-targeted tyrosine kinase inhibitor (TKI) that inhibits angiogenesis by targeting VEGFR, FGFR, and PDGFR; **benmelstobart** (TQB2450), a humanized monoclonal antibody that blocks the Programmed cell death 1 ligand 1 (PD-L1) to restore anti-tumor immune responses; and the standard-of-care chemotherapy doublet **cisplatin** and **gemcitabine**. The rationale for this combination is to leverage the anti-angiogenic and immunomodulatory effects of anlotinib and the cytotoxic debulking of chemotherapy to enhance the efficacy of PD-L1 inhibition. The regimen is primarily developed by Chia Tai Tianqing (Sino Biopharmaceutical) and is being evaluated in clinical trials led by institutions such as the Sun Yat-sen University Cancer Center.

Other names
TQB2450 + anlotinib + gemcitabine + cisplatinTQB2450 + anlotinib + GC
02

Targets

DNAFGFR1 (Fibroblast growth factor receptor 1)CD274 (Programmed cell death protein 1 ligand 1)PDGFRB (Platelet-derived growth factor receptor beta)VEGFR2 (Vascular endothelial growth factor receptor 2)VEGFR4 (Vascular endothelial growth factor Receptor-3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)FGFR2 (Keratinocyte growth factor receptor)FGFR3 (Fibroblast growth factor receptor 3)FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)RNR (Ribonucleotide reductase)VEGFR-1 (Vascular endothelial growth factor receptor 1)

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