Drug intelligence / Profile preview

JSKN033 (Alphamab Oncology)

Development stage
Unknown
Lead developer
AlphaMab Oncology
Modality
Bispecific Antibodies → Multispecific Antibodies → Engineered Antibody Formats → Antibody-Based Therapeutics, Fc-Fusion Proteins → Carrier/Scaffold Proteins → Recombinant Proteins and Enzymes, Nanobodies (VHH) → Antibody Fragments → Engineered Antibody Formats → Antibody-Based Therapeutics, Cytotoxic ADCs → Antibody-Drug Conjugates (ADCs) → Antibody Conjugates → Antibody-Based Therapeutics
Administration
Subcutaneous
01

Overview

JSKN033 is a first-in-class, high-concentration subcutaneous co-formulation developed by Alphamab Oncology for the treatment of advanced metastatic malignant tumors. It consists of two active components: JSKN003, a bispecific antibody-drug conjugate (ADC) targeting two non-overlapping epitopes of the HER2 extracellular domain, and envafolimab, a humanized anti-PD-L1 single-domain antibody (sdAb) Fc fusion protein. JSKN003 utilizes a cleavable linker and a topoisomerase I inhibitor payload to induce targeted tumor cell death. By combining the direct cytotoxic effects of the ADC with the immune checkpoint inhibition provided by envafolimab, JSKN033 leverages a dual mechanism of action to enhance anti-tumor efficacy. It is currently being evaluated in Phase I/II clinical trials for HER2-positive and PD-L1-expressing solid tumors, including cervical cancer and non-small cell lung cancer.

02

Targets

ERBB2 (Erb-b2 receptor tyrosine kinase 2)CD274 (Programmed cell death protein 1 ligand 1)TOP1 (DNA Topoisomerase I)

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