Drug intelligence / Profile preview

JSKN016 + docetaxel

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

Overview

JSKN016 + docetaxel is an investigational combination therapy composed of JSKN016, a bispecific antibody-drug conjugate (ADC) targeting HER3 (Human epidermal growth factor receptor 3) and TROP2 (Trophoblast cell surface antigen 2), and docetaxel, a well-established chemotherapy agent. JSKN016 is developed using Alphamab Oncology’s proprietary Glycan-specific conjugation platform. Upon binding to TROP2 and/or HER3 on tumor cells, JSKN016 is internalized via endocytosis, releasing a cytotoxic topoisomerase I inhibitor (TOPIi), which triggers apoptosis in TROP2/HER3-positive tumor cells and presents a bystander effect by affecting adjacent antigen-negative tumor cells. Docetaxel is a cytotoxic taxane chemotherapy that inhibits cell division by stabilizing microtubules. The combination is being evaluated in clinical studies for efficacy and safety in advanced solid tumors, including non-small cell lung cancer (NSCLC) and HER2-negative breast cancer[1][2][3][4][5].

02

Targets

TOP1 (DNA Topoisomerase I)TACSTD2 (Tumor-associated calcium signal transducer 2)TUBB (Tubulin (alpha and beta subunits))ERBB3 (Erb-b2 receptor tyrosine kinase 3)

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