Engineering precision genetic therapies
We engineer precision medicines with gene-encoding single-stranded DNA for a variety of in vivo therapeutic applications.
What if gene delivery did not require an external carrier?
Using computational design, our novel targeting gene carriers are constructed with single-stranded DNA that folds around its main cargo, the therapeutic single-stranded DNA it is delivering to target cells. These non-viral, non-LNP carriers are non-toxic, non-immunogenic, and non-inflammatory. They can be constructed to encode for virtually any gene of interest and for precise in vivo tissue and cell targeting. Importantly, using proprietary process innovations, we can manufacture the gene carriers in a scalable fashion.
Our novel gene carrier unlocks an entirely new approach to in vivo gene delivery, overcoming critical limitation of existing viral and non-viral gene delivery technologies such as immunogenicity, inflammation and reactogenicity, poor targetability, and tedious manufacturing which have held back the genetic medicines field from bringing critical therapies to patients.
Programmed precision
Genetic medicines engineered with single-stranded DNA allow unprecedented precision and control, enabling innovative approaches to important therapeutic challenges, such as in vivo treatments for cancer.
This proprietary technology can be applied across modalities for the shape, size, number of copies, spacing, payload type, bio- and tissue localization, and more...

Carrier technology
- Genetic Payload (DNA, mRNA)
- Genetic Cell + Tissue Recognition Effectors/Engagers (DNA, mRNA)
- Small Molecule Drugs & Peptides
- Proteins & Antibodies
Removing Barriers in Drug Discovery & Development
- Construct novel treatments
- Increase specificity
- Co-deliver drugs and genes
- Repurpose drugs for new indications
- Enhance efficacy of existing drugs