This poster highlights a novel approach to antisense architecture using transient cyclic structures designed to improve potency, reduce immune activation, and enhance the overall drug-like properties of RNA therapeutics. Download the poster to see how cyclic design can help overcome limitations of traditional linear ASOs.
In this poster, you’ll See:
The design rationale behind AntiClastic™ cyclic antisense oligonucleotides
How 3’-3’ and 5’-5’ cyclic linkages influence biological performance
Data demonstrating improved potency compared to conventional gapmers
Evidence of reduced immune activation and improved safety profile
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Discover more about Genetic Medicines at Alloy
Shaping the RNA Century
Improved Potency: The AntiClastic cyclic and 5’ end-engineering results in up to a 50-fold improvement in in vitro potency.
Increased Patient Safety:Reduced engagement of off-target RNA and pattern recognition receptors mitigates the inflammatory response, thereby improving the therapeutic index.
IP Protection:The AntiClastic platform creates novel, globally IP-protected therapeutic structures.
Clinically Validated Methods:Manufactured using conventional chemical methods and engineered with building blocks of clinically validated and established oligonucleotide therapeutic modifications.