Drug intelligence / Profile preview

VBC101

Development stage
Phase 2
Lead developer
VelaVigo
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

VBC101 is a novel bispecific antibody-drug conjugate designed for the treatment of advanced solid tumors. Developed by VelaVigo, it targets both Epidermal Growth Factor Receptor (EGFR) and c-Met, two important oncogenic drivers frequently overexpressed in solid tumors. VBC101 functions as a mitosis inhibitor, most likely through an auristatin toxin payload conjugated to the bispecific antibody backbone. It acts by binding to and inhibiting EGFR and c-Met, leading to targeted cytotoxicity in cancer cells expressing these antigens. The drug is currently in preclinical and early clinical development, with a first-in-human Phase 1/2a clinical trial planned for advanced solid tumor malignancies[1][2][3][5].

02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)MET (Mesenchymal-epithelial transition factor receptor)

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