Drug intelligence / Profile preview

CRISPR-Cas9-LNP

Development stage
Preclinical
Lead developer
InhaTarget Therapeutics
Modality
CRISPR-Cas9 → CRISPR Systems → Programmable Nucleases → Gene Editing → Gene Therapies, Lipid-based Nanoparticles → Nanoparticles → Drug Delivery Systems
Administration
Inhalation
01

Overview

CRISPR-Cas9-LNP is a research-stage, inhaled gene-editing therapeutic candidate being developed by InhaTarget Therapeutics for the treatment of squamous non-small cell lung cancer (NSCLC). The therapeutic approach utilizes lipid nanoparticles (LNPs) to deliver CRISPR-Cas9 gene-editing machinery directly to the lungs via inhalation. This localized delivery method is designed to target and reprogram tumor-associated macrophages (TAMs) or directly target tumor cells, bypassing systemic toxicities associated with intravenous administration. While the specific gene target for this program has not been publicly disclosed, the platform aims to modulate the tumor microenvironment to overcome treatment resistance and inhibit tumor progression.

02

Targets

DNA

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