Drug intelligence / Profile preview

trastuzumab + LCN2 siRNA

Development stage
Preclinical
Modality
Chemically Modified siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Conjugated siRNA → Small Interfering RNA (siRNA) → Small RNA Therapeutics → RNA Therapeutics → Nucleic Acid Therapeutics, Monoclonal Antibodies → Antibody-Based Therapeutics
Administration
Intravenous, Systemic Delivery, Nanoparticle-based Delivery
01

Overview

This combination drug consists of trastuzumab, a monoclonal antibody targeting the human epidermal growth factor receptor type 2 (HER2), and a small interfering RNA (siRNA) designed to knock down Lipocalin-2 (LCN2) expression. Trastuzumab inhibits HER2 receptor signaling, leading to decreased proliferation in HER2-overexpressing tumors, particularly in breast cancer. LCN2 siRNA targets and reduces LCN2 gene expression using RNA interference, which has been shown to decrease cell proliferation and invasion in experimental models. The combination aims to address drug resistance in HER2-positive cancers, especially breast cancer, by simultaneously blocking HER2 signaling and LCN2-mediated pathways, potentially enhancing antitumor efficacy in cases where resistance to trastuzumab develops[1][6].

02

Targets

LCN2 (Lipocalin-2)ERBB2 (Erb-b2 receptor tyrosine kinase 2)

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