The awarded project, ASO Connect, aims to make ASOs (antisense oligonucleotides) more accessible to children and youth with rare diseases. ASOs are a promising new approach to treat genetic conditions. They are short, synthetic, single-stranded molecules designed to bind to RNA. This binding can regulate harmful transcripts, correct splicing errors, or increase protein expression to help treat rare diseases.
“We are excited by the prospect of ASO treatment because they are customizable to individual patients and their unique genetic differences,” says Costain, Co-lead of Advanced Therapeutics, Staff Physician, Scientist, Genetics & Genome Biology, SickKids. “However, there are still major challenges in expanding access, identifying eligible children and designing ASOs for testing.”
With the funding, the team plans to facilitate more proactive identification of children with genetic diagnoses that might be amenable to ASO treatment. Additionally, they aim to design ASO sequences in advance so they can be rapidly tested, speeding up pre-clinical development and ensuring scalability through an open-access platform.
“ASO Connect is a transformative step towards targeted treatment and better outcomes for children at both centres and beyond,” says Campeau, Geneticist and clinician-scientist, Centre de recherche Azrieli, CHU Sainte-Justine. “We have the opportunity to change the paradigm, and with this funding, we will.”
The Translational Program was made possible through the Azrieli Foundation, whose transformational gift fuels the partnership.
Working together, the PCHP aims to unlock a flourishing discovery and research eco-system between the two institutions, unleashing the potential of Precision Child Health.
Source: SickKids