Drug intelligence / Profile preview

vebecotutamab + lenvatinib

Development stage
Unknown
Lead developer
MacroGenics
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Small Molecules
Administration
Intravenous, Oral
01

Overview

vebecotutamab + lenvatinib is a combination therapy being investigated for the treatment of salivary gland carcinoma. Vebecotutamab (MGD019) is a bispecific DART (Dual-Affinity Re-Targeting) molecule designed to simultaneously target and block the immune checkpoint receptors PD-1 and CTLA-4, thereby enhancing T-cell activation and anti-tumor immune responses. Lenvatinib is an oral multi-receptor tyrosine kinase inhibitor that targets vascular endothelial growth factor receptors (VEGFR1-3), fibroblast growth factor receptors (FGFR1-4), platelet-derived growth factor receptor alpha (PDGFRα), KIT, and RET. By combining dual checkpoint blockade with anti-angiogenic and anti-proliferative kinase inhibition, this regimen aims to overcome tumor-induced immunosuppression and inhibit tumor growth and vascularization. It is currently being evaluated in a Phase 2 umbrella trial sponsored by Peking Union Medical College for patients with locally advanced, recurrent, or metastatic salivary gland carcinoma.

Brand names
Lenvima
Other names
MGD019 + lenvatinibvebecotutamab ± lenvatinib
02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)KIT (c-KIT proto-oncogene receptor tyrosine kinase)PDCD1 (Programmed cell death protein 1 receptor)FGFR3 (Fibroblast growth factor receptor 3)CTLA-4 (Cytotoxic t-lymphocyte–associated protein 4)VEGFR3 (Vascular endothelial growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR2 (Vascular endothelial growth factor receptor 2)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FGFR2 (Keratinocyte growth factor receptor)

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