Drug intelligence / Profile preview

anti-EpCAM-AAV2 + shEGFR

Development stage
Preclinical
Modality
Viral Vectors → Gene Addition/Replacement → Gene Therapies, Viral-delivered RNAi → In Vivo RNAi → Gene Silencing → Gene Therapies, Antibody-Based Therapeutics
Administration
Intravenous
01

Overview

A combination **gene therapy platform** consisting of a modified adeno-associated virus serotype 2 (**AAV2**) vector conjugated to an anti-EpCAM antibody for tumor targeting, and encoding a short hairpin RNA (**shRNA**) that silences epidermal growth factor receptor (**EGFR**) expression. The anti-EpCAM antibody directs the viral vector to **EpCAM-positive tumor cells**, enabling tumor-specific delivery. Upon systemic administration, the vector delivers shEGFR to tumor cells for **long-term EGFR knockdown**, leading to **inhibition of tumor growth** in EpCAM+ cancers (e.g., ovarian cancer). The construct utilizes a **streptavidin-biotin bridge** for conjugation and demonstrates enhanced selectivity for tumor tissue and reduced off-target effects. This agent is experimental and has not been approved for clinical use[1].

Other names
anti-EpCAM antibody-conjugated AAV2/shEGFRanti-EpCAM-AAV2/shEGFR vector
02

Targets

EGFR T790M (Epidermal growth factor receptor T790M mutant)EPCAM (Epithelial cell adhesion molecule)

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