Drug intelligence / Profile preview

BL-B16D1

Development stage
Phase 1
Lead developer
Biokin Pharmaceutical
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

BL-B16D1 is an investigational antibody-drug conjugate (ADC) that targets both the epidermal growth factor receptor (EGFR) and human epidermal growth factor receptor 3 (HER3/ERBB3). It is designed as a dual-antibody ADC, meaning it simultaneously binds to EGFR and HER3 on tumor cells, delivering a cytotoxic payload via a new generation of toxins. The drug is being developed for the treatment of advanced solid tumors, including unresectable locally advanced or metastatic breast cancer, head and neck cancer, squamous cell carcinoma, and other solid tumors. Its mechanism of action involves inhibiting EGFR and ERBB3 signaling pathways while delivering targeted cytotoxicity through its conjugated toxin.

02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)ERBB3 (Erb-b2 receptor tyrosine kinase 3)

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