Future of gene-based medicines

EVis Bioscience is an ETH spin-off developing a next-generation non-viral vector for targeted gene therapy.

A pioneer approach to treating genetic disorders

We develop innovative gene delivery systems for targeted and personalized medicine.
This includes extracellular vesicles, synthetic lipid nanoparticles, and their hybrids.

Gene delivery

Novel opportunities to deliver small and large nucleic acids using extracellular vesicles for targeted and personalized medicine

Internal pipeline

Development of gene therapy-based candidates for rare genetic diseases

Vehicle sublicenses

We offer our proprietary hybrid technology to pharmaceutical partners to support the development of targeted gene-based therapies

Service

We provide services and facilities to research labs focused on the delivery of nucleic acids using extracellular vesicles

RNA loading kit: NanoVector

We offer our chemical kit to load your EVs with small and large RNAs, protecting the EV structure and biological activity

Fluorescent kit

We offer our fluorescent kit to track EVs in tube and in vitro, protecting the EV structure and biological activity

TECHNOLOGY

Next-Generation RNA Delivery

Our patented NanoVector platform enables safer, targeted, extrahepatic delivery beyond current viral and non-viral systems.

MARKET

The global gene therapy market is expanding rapidly, creating strong demand for more precise and scalable delivery technologies.

IMPACT
Our approach opens new therapeutic opportunities for patients with genetic disorders lacking effective treatments today.
MOMENTUM

A scalable, low-toxicity platform already attracting scientific interest and moving toward market readiness. Ready for Commercialization by 2026

Supported by

Partner with Us

We develop our drug product and support pharmaceutical partners by providing our hybrid technology to enable innovative gene therapies for patients.


JOIN THE INNOVATION

We develop our drug product and support pharmaceutical partners by providing our hybrid technology to enable innovative gene therapies for patients.