Drug intelligence / Profile preview

JSKN016

Development stage
Phase 3
Lead developer
AlphaMab Oncology
Modality
Small Molecules, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

JSKN016 is a bispecific antibody-drug conjugate (ADC) developed by Alphamab Oncology using a proprietary Glycan-specific conjugation platform. It simultaneously targets HER3 (Human epidermal growth factor receptor 3) and TROP2 (Trophoblast cell surface antigen 2) on tumor cells. Upon binding to these antigens, JSKN016 is internalized via target-mediated endocytosis, where it releases a cytotoxic topoisomerase I inhibitor (TOPIi), inducing apoptosis in HER3- or TROP2-positive tumor cells. The released inhibitor can also permeate neighboring antigen-negative tumor cells, exerting a bystander effect and further inhibiting tumor growth. JSKN016 is currently being evaluated in phase I clinical trials for the treatment of advanced malignant solid tumors in China.

02

Targets

TACSTD2 (Tumor-associated calcium signal transducer 2)ERBB3 (Erb-b2 receptor tyrosine kinase 3)

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