Investors
Why Invest in
Genexys BioMed?
Genexys BioMed is pioneering a next-generation gene therapy platform designed to overcome the challenges of viral and LNP gene delivery. We are advancing toward clinical trials with a transformative approach to treating cystic fibrosis (CF) and other genetic diseases.

Investment Highlights
Genexys BioMed isn’t just developing a treatment—we’re redefining the future of genetic medicine.
Large and Growing Market Opportunity
The global CF market was $5.75 billion in 2021 and is expected to grow at 24.3% CAGR through 2030, creating strong demand for curative therapies.
Addressing an Urgent Medical Need
Our lead program, GEN-023, is specifically designed for the final 10% of CF patients (~3,000 in the U.S.) who cannot benefit from existing treatments– representing a critical, underserved population.
Proven Technology with Clinical Precedent
A Phase 1 clinical trial using a related delivery system demonstrated no serious adverse events (SAEs) and clinically significant CFTR function restoration– providing a strong foundation for GEN-023’s success.
Breakthrough Gene Therapy Platform
Our non-viral, non-LNP GeneZip system overcomes the limitations of traditional gene therapy, allowing for repeat dosing, enhanced delivery, and long-term safety.
Strong Financial & Strategic Backing
Backed by Orange Grove Bio support from the NIH (NHLBI), we are well-positioned to accelerate preclinical development and first-in-human trials.
Beyond CF—A Scalable Gene Therapy Platform
The GeneZip platform extends beyond CF, with broad applications in neurological and large-gene diseases. Preclinical studies have already demonstrated long-term gene expression in a variety of tissues, opening doors for multiple high-value indications.
Recent News
Read about our latest developments, including funding rounds, partnership announcements, and progress in our pipeline.