Drug intelligence / Profile preview

BL-B01D1 + lenvatinib

Development stage
Unknown
Lead developer
SystImmune
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous, Oral
01

Overview

BL-B01D1 + lenvatinib is an investigational combination therapy comprising BL-B01D1, a first-in-class bispecific antibody-drug conjugate (ADC) targeting both EGFR (epidermal growth factor receptor) and HER3 (human epidermal growth factor receptor 3), and lenvatinib, an approved multi-targeted tyrosine kinase inhibitor. BL-B01D1 works by simultaneously binding to EGFR and HER3 on tumor cells, blocking proliferative and survival signaling, and delivering a cytotoxic payload upon internalization to induce cancer cell death. Lenvatinib inhibits multiple receptor tyrosine kinases involved in tumor angiogenesis and progression, including VEGFR, FGFR, PDGFRα, RET, and KIT. This combination is under clinical investigation for advanced hepatocellular carcinoma and additional solid tumor types[1][2][3][4][5][6].

02

Targets

FGFR4 (Fibroblast growth factor receptor 4)PDGFRA (Platelet-derived growth factor receptor alpha)ERBB3 (Erb-b2 receptor tyrosine kinase 3)KIT (c-KIT proto-oncogene receptor tyrosine kinase)VEGFR2 (Vascular endothelial growth factor receptor 2)PDGFRB (Platelet-derived growth factor receptor beta)TOP1 (DNA Topoisomerase I)FGFR3 (Fibroblast growth factor receptor 3)VEGFR-1 (Vascular endothelial growth factor receptor 1)VEGFR3 (Vascular endothelial growth factor receptor 3)EGFR T790M (Epidermal growth factor receptor T790M mutant)FGFR1 (Fibroblast growth factor receptor 1)RET (Rearranged during transfection receptor tyrosine kinase)FGFR2 (Keratinocyte growth factor receptor)

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