Genetic Medicines Inspired by Nature

Revolutionizing Gene Therapy With Non-Viral Delivery Methods for Stargardt's, ALS, Alzheimer’s, Duchenne & other Systemic Diseases

Pioneering Non-Viral Gene Delivery

At AAVINUE, we are driven by a vision to revolutionize gene therapy for debilitating diseases using our proprietary Mini-nucleosome non-viral delivery technology. Our work is dedicated to overcoming the challenges of viral vectors and LNPs to enable transformative therapies for conditions like ALS, Stargardt's, Alzheimer’s Disease, and other genetic diseases.

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Patient Focused

Patient first mentality drives our entire drug development process.

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Cutting-Edge Technology

Leader in non-viral gene Delivery and Cargo technologies.

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Robust Platforms

Customizable for targeted delivery of DNA/RNA to treat diverse diseases

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Designed for Success

Highly accessible to patients via friendly economics

Scientists analyzing samples in a laboratory setting.

Collaborative Innovation and Approach

Backed by a team of seasoned experts in neuroscience, ophthalmology gene therapy, and biotech entrepreneurship, AAVINUE has developed scalable gene therapy solutions already for high unmet need diseases. Our approach is grounded in rigorous science and strengthened through collaborations with world-class academic investigators.

Nature-Inspired Breakthroughs

With a robust intellectual property portfolio and long patent life, AAVINUE is positioned to lead the next wave of breakthroughs in non-viral gene therapy.

  • Mini-nucleosome emulates how nucleic acids are chromatinized in human cells
  • Our therapeutic targets are genetically validated
  • Possibility to deliver a combination of genes to treat multiple aspects of the disease with one vector

Our Pipeline

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Scientist examining blue liquid in flask.

Transforming the Future

Join us in transforming the future of ophthalmic and neurodegenerative disease treatment—without the virus. Reach out to us for more information.