Drug intelligence / Profile preview

BG-C0902

Development stage
Phase 1
Lead developer
BeOne Medicines
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

BG-C0902 is a bispecific antibody-drug conjugate (ADC) developed by BeOne Medicines for the treatment of advanced solid tumors. It consists of a fully humanized bispecific antibody targeting both the Epidermal Growth Factor Receptor (EGFR) and the Hepatocyte Growth Factor Receptor (MET). The antibody is conjugated via an enzymatically cleavable linker to a topoisomerase 1 (TOPO1) inhibitor payload. By simultaneously targeting EGFR and MET, BG-C0902 is designed to overcome resistance mechanisms often encountered with single-target therapies, particularly in tumors where these pathways are co-activated or where one pathway compensates for the inhibition of the other. The drug is currently undergoing Phase 1a/1b clinical evaluation to assess its safety, pharmacokinetics, and preliminary antitumor activity in patients with advanced solid tumors.

02

Targets

TOP1 (DNA Topoisomerase I)EGFR T790M (Epidermal growth factor receptor T790M mutant)MET (Mesenchymal-epithelial transition factor receptor)

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