Drug intelligence / Profile preview

BG-C477 + tislelizumab

Development stage
Phase 1
Lead developer
BeOne Medicines
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

BG-C477 + tislelizumab is an investigational combination regimen consisting of BG-C477, a novel antibody-drug conjugate (ADC) targeting carcinoembryonic antigen-related cell adhesion molecule 5 (CEACAM5/CEA), and tislelizumab, a humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1). Developed by BeOne Medicines (formerly BeiGene), BG-C477 comprises a CEA-specific antibody conjugated to a topoisomerase I inhibitor payload via a cleavable linker, designed to deliver cytotoxic therapy directly to CEA-expressing tumor cells while inducing bystander killing of neighboring tumor cells. Tislelizumab acts as an immune checkpoint inhibitor, blocking the interaction of PD-1 with its ligands PD-L1 and PD-L2 to restore T-cell-mediated antitumor activity. The combination is being evaluated in a Phase 1a/1b clinical trial (NCT06596473) for the treatment of selected advanced solid tumors.

Other names
BG-C477 + BGB-A317BG-C477 and tislelizumabBG-C-477 and tislelizumabBG-C 477 and tislelizumabBG-C477 in combination with tislelizumabBG-C-477 in combination with tislelizumabBG-C 477 in combination with tislelizumabtislelizumab + BG-C477
02

Targets

CEACAM5 (Carcinoembryonic antigen related cell adhesion molecule 5)PDCD1 (Programmed cell death protein 1 receptor)

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