Drug intelligence / Profile preview

JSKN016SC

Development stage
Phase 1
Lead developer
AlphaMab Oncology
Modality
Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics, Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics
Administration
Subcutaneous
01

Overview

JSKN016SC is a subcutaneous formulation of JSKN016, a bispecific antibody-drug conjugate (ADC) developed by Alphamab Oncology (Jiangsu Alphamab Biopharmaceuticals). It simultaneously targets Human Epidermal Growth Factor Receptor 2 (HER2) and Human Epidermal Growth Factor Receptor 3 (HER3). The drug utilizes Alphamab's proprietary glycan-fixation site-specific conjugation platform to attach a cytotoxic payload, typically a topoisomerase I inhibitor, to the bispecific antibody. This dual-targeting approach is designed to enhance tumor specificity and overcome resistance mechanisms associated with single-target HER2 or HER3 therapies. The subcutaneous administration route is being evaluated for its potential to improve patient convenience and provide a distinct pharmacokinetic profile compared to traditional intravenous ADC delivery. It is currently in early-phase clinical development for advanced solid tumors, including non-small cell lung cancer (NSCLC) with EGFR mutations and HER2-negative breast cancer.

02

Targets

ERBB3 (Erb-b2 receptor tyrosine kinase 3)TACSTD2 (Tumor-associated calcium signal transducer 2)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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