Sharing Insight for Gene Therapy Manufacturing
Converting vertical information approaches into horizontal solutions for all members of the rare disease community....
About Odylia
Our Path
Resources
Consortium
What we do
Odylia Therapeutics is a non-profit corporation working to bring treatments for rare eye disease from the lab into humans using genetic therapies. Today, there are more than 300 known genetic forms of Inherited Retinal Disease (IRD) that lead to blindness, with some of these interfering with other sensory mechanisms like hearing and balance. Most are extremely rare, impacting less than one in a million people worldwide.
Why we exist
Although pre-clinical proof-of-concept treatments exist for some of these diseases, because they are so rare, there is little commercial interest in them. Odylia was formed to find a way to move these potential therapies into clinical trials to protect and restore the vision of those going blind.
Why we exist
Although pre-clinical proof-of-concept treatments exist for some of these diseases, because they are so rare, there is little commercial interest in them. Odylia was formed to find a way to move these potential therapies into clinical trials to protect and restore the vision of those going blind.
Latest news
Stay up-to-date with our research and clinical trials
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Meet up at the JP Morgan Healthcare Conference
Meet members of the Odylia team at the JP Morgan Healthcare Conference. We would love to connect....
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Ashley Winslow joins the Odylia team
Dr. Winslow will oversee scientific operations and strategy development with a focus on expanding partnerships....