mission: to deliver safe, precise, and repeatable treatments for patients with severe genetic disorders.
Vision: Harness innate cellular enzymes to correct faulty genes without introducing foreign nucleases.
Prevent Double-Strand Breaks: lower genomic instability risk
Enable Re-dosing: Minimized immune response allows repeated treatments over a patient’s lifetime.
Expand Target Range: No reliance on PAM sequences, so we can edit broader genomic loci.
Preserve Safety: Long guide RNAs (30 > bases) ensure pinpoint accuracy with negligible off-target edits.
No DSBs due to Cas-free platform
More flexible targeting for broader therapeutic pipeline
Non-viral delivery enables repeat dosing
Multiple mutation types corrected on one platform