Drug intelligence / Profile preview

BM230 + tislelizumab

Development stage
Unknown
Lead developer
Biomissile Pharmaceuticals
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Nanobodies (VHH) → Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

BM230 + tislelizumab is an investigational combination therapy comprising BM230, a fully human bispecific nanobody targeting Human Epidermal Growth Factor Receptor 2 (HER2), and tislelizumab, a humanized IgG4 monoclonal antibody that inhibits Programmed Cell Death Protein 1 (PD-1). Developed by Suzhou Biomissile Pharmaceuticals, BM230 is designed to bind to HER2-expressing tumor cells to inhibit their proliferation, while tislelizumab acts as a checkpoint inhibitor to prevent the interaction between PD-1 and its ligands (PD-L1 and PD-L2), thereby restoring the anti-tumor activity of T cells. The combination is currently undergoing Phase Ib/II clinical evaluation for the treatment of HER2-related advanced solid tumors, including colorectal, esophageal, and urothelial cancers.

Other names
BM230 + PD-1 inhibitor
02

Targets

PDCD1 (Programmed cell death protein 1 receptor)FCGRT (Neonatal crystallizable fragment receptor)FcγR (Low affinity immunoglobulin gamma Fc region receptor II-c)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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