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Drug intelligence / Profile preview
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.
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