Drug intelligence / Profile preview

BB-205

Development stage
Preclinical
Lead developer
Bright Biologics
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

BB-205 is a novel bispecific antibody-drug conjugate (ADC) designed to target two tumor-associated antigens: human epidermal growth factor receptor 2 (HER2) and hepatocyte growth factor receptor (c-Met). Developed by Bright Biologics, the molecule is engineered using humanized anti-HER2 and anti-c-Met VHH fragments fused with a human IgG1 Fc region. It is conjugated to the microtubule inhibitor monomethyl auristatin E (MMAE) via a cathepsin-cleavable valine-citrulline (vc) linker. BB-205 is intended to address tumor heterogeneity and potential escape mechanisms by dual-targeting antigens that are often co-expressed or separately expressed in various solid tumors, including lung, pancreatic, and kidney cancers. In preclinical studies, BB-205 demonstrated superior cytotoxicity and higher internalization rates compared to single-target reference ADCs in dual-expressing cancer cell lines. In vivo xenograft models for pancreatic and lung cancer showed significant tumor growth inhibition and high rates of tumor-free survival following treatment.

02

Targets

TUBB (Tubulin (alpha and beta subunits))MET (Mesenchymal-epithelial transition factor receptor)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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