
06/04/2025
As researchers continue to discover new gene variants linked to inherited blindness, the case for mutation-agnostic therapies grows stronger.
A recent study from the University of Oklahoma uncovered 20 newly identified gene variants in retinal disease – adding to an already complex genetic landscape.
While gene therapies remain a potentially powerful approach, they are often specific to a particular mutation. That’s why we’re developing KIO-301: a mutation-agnostic small molecule designed to restore light perception regardless of the underlying genetics.
It’s not about replacing gene therapies – but expanding options for patients. Mutation-agnostic approaches like 301 can work alone or alongside gene therapy, creating a more inclusive future for patients.
🔗 Read the study: https://eyewire.news/news/university-of-oklahoma-study-identifies-20-novel-variants-for-inherited-retinal-diseases?c4src=article:infinite-scroll
🔬 Learn about KIO-301: https://bit.ly/Kiora_Home