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- Novel circVec 3.0 design feature achieves 27- and 4-fold improvement vs. circVec 1.1 and 2.1 generation, respectively
- circVec circular mRNA shows up to 75 times longer half-life than conventional linear mRNA in vivo
- Muscle-specific circVec 2.0-AAV vectors validated by systemic delivery in vivo
- The results will be discussed in a live webcast at 10am CEST on 4 December 2024
Oslo, Norway 4 December 2024 - Circio Holding ASA (OSE: CRNA), a biotechnology company developing powerful circular RNA technology for next generation nucleic acid medicine, today announces an R&D update showcasing the latest powerful circVec 3.0 generation circular mRNA expression system and bioinformatic analysis of long-term expression data in mouse muscle. The analysis demonstrates up to 75 times prolonged half-life vs linear mRNA in vivo.
"With Circio's circVec 2.1 construct we have already demonstrated the potential of our powerful circular RNA technology to outperform mRNA-based expression systems both in vitro and in vivo. Continued optimization of the circVec genetic cassette has now resulted in the discovery of a novel enhancer element, which brings up to 27- and 4-fold improvement over the previous circVec 1.1 and 2.1 generations, respectively. This new component will be added as a standard design feature in circVec generation 3.0," said Dr. Thomas B Hansen, CTO at Circio. "We are very eager to explore how this new feature can further boost circVec protein expression level and durability in vivo, with the aim to improve potency and safety of nucleic acid medicines. Our science team is now rapidly advancing to implement the new circVec 3.0 design into AAV and DNA-based vector formats for future therapeutic applications."
In addition, Circio presents bioinformatic analysis of long-term in vivo expression data showing an estimated circular mRNA half-life of more than 600 hours vs. less than 10 hours for linear mRNA in mouse muscle. This translates to up to 75 times prolonged half-life in vivo, substantially higher than the 15 times enhancement previously reported in vitro.
"Reaching this level of unprecedented RNA half-life in vivo, combined with the added power of circVec generation 3.0, represents the latest major milestone for our circular mRNA expression platform," said Dr. Erik Digman Wiklund, CEO at Circio. "We are demonstrating that our technology has the potential to substantially enhance current gold-standard nucleic acid medicines, and bring benefit to patients with difficult-to-treat diseases for which there are no cures available today."
Circio also reports interim in vivo results for the AAV gene therapy vector format. Protein expression from an AAV9 construct with the circVec 2.0 genetic cassette has now been validated by systemic administration in vivo, showing a similar expression pattern to current gold-standard mRNA-AAV for the first 30 days. The experiment is continuing, and previous evidence suggests that the circVec expression advantage usually emerges 4 weeks after injection and then increases over time. circVec generation 3.0 AAV constructs are currently being designed and will enter in vivo testing during 1Q 2025.
The circVec 3.0 data and recent in vivo results will be presented and discussed by Circio management in a live webcast at 10:00am CEST on 4 December 2024. A recording of the webcast will be made available on the Circio webpage.