Drug intelligence / Profile preview

obinutuzumab beta (Beijing Tianguangshi Pharmaceutical Technology)

Development stage
Phase 2
Lead developer
Beijing Tianguangshi Pharmaceutical Technology
Modality
Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

Beijiexin (obinutuzumab beta, development code MIL62) is an innovative, glycoengineered, type II anti-CD20 monoclonal antibody developed by Beijing Mabworks Biotech. It is designed with a near-completely afucosylated Fc region to significantly enhance its binding affinity to FcγRIIIa receptors on immune effector cells, thereby boosting antibody-dependent cellular cytotoxicity (ADCC) and B-cell depletion. As a type II anti-CD20 antibody, it also promotes direct B-cell death rather than complement-dependent cytotoxicity. Beijiexin is approved in China for the treatment of neuromyelitis optica spectrum disorder (NMOSD) and primary membranous nephropathy (pMN), making it the first domestically developed third-generation CD20 antibody approved in China and the world's first targeted therapy specifically approved for pMN. It is also in clinical development for various other autoimmune diseases and B-cell malignancies, including follicular lymphoma, systemic lupus erythematosus, and lupus nephritis.

Brand names
BeijiexinBejescin倍捷欣
Other names
obinutuzumab beta injectionobinutuzumab βotuzumab betaotuzumab beta injectionotuzumab βotuzumab β injection奥妥珠单抗β奥妥珠单抗β注射液重组人源化单抗MIL62
02

Targets

C1Q (Complement C1q)CD20 (B-lymphocyte antigen CD20)FCGR3A (Low affinity immunoglobulin gamma Fc region receptor III-A)FCGR3B (Low affinity immunoglobulin gamma Fc region receptor III-B)

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