To continue in our support of Odylia and finding a treatments for our daughters condition, Lebers Congenital Amaurosis.

Freya is a happy, caring ,fun, bright 9 year old girl, who loves baking, crafts, reading, horse riding and raising money for different charities and causes as she loves to help others.

Watching Freya you probably wouldn’t realise that she is registered visually impaired, having been born with Nystagmus, which causes blurred and incentive vision, and LCA (lebers congenital amourosis) RGRIP1 gene which is a degenerative condition.

As Freya’s parents (Gav & Paula Birch) we hope and pray that treatment can become available to prevent this and retain her vision

The support we have had over the years is amazing, and our hopes are for it to continue and grow bigger and stronger.

Odylia Therapeutics is a charity developing a gene therapy to treat vision loss caused by RPGRIP1 mutations, for which there is currently no treatment. Odylia partners with patients, families, and researchers all over the world to accelerate therapeutic development and is currently conducting late-stage preclinical experiments and is preparing for IND submission for use of the gene therapy in clinical trials.

Odylia’s focus starts and ends with patients. We are committed to changing the future for families affected by rare disease around the world. YOU can help bring promising treatments to patients. You can donate from this page - donations are made in USD ($) but then will be converted converted on the backend to GBP which you will see on your statement after the transaction.

At Odylia, we accelerate therapeutic development for people with rare diseases, changing the way treatments are brought from the lab to the clinic. We strive to bring life altering treatments to people with genetic disease regardless of prevalence or commercial interest. Odylia is shifting the paradigm to focus on proven science and removing traditional roadblocks. We work to lower costs, reduce development time, focus research, and continuously drive successful programs towards clinical trials and regulatory approval. Strategic collaborations with patient groups, research labs, and commercial partners facilitate our work to ensure treatments are safe, effective, and ultimately reach patients who need them.

SUPPORTING FREYA’S SIGHT

Odylia Therapeutics is a nonprofit biotech working to accelerate the development of treatments for people with rare diseases.

At Odylia, we accelerate therapeutic development for people with rare diseases, changing the way treatments are brought from the lab to the clinic. We strive to bring life altering treatments to people with genetic disease regardless of prevalence or commercial interest. 
Odylia is shifting the paradigm to focus on proven science and removing traditional roadblocks. We work to lower costs, reduce development time, focus research, and continuously drive successful programs towards clinical trials and regulatory approval. Strategic collaborations with patient groups, research labs, and commercial partners facilitate our work to ensure treatments are safe, effective, and ultimately reach patients who need them.

Odylia challenges the traditional approach to drug development through:

1. Lower cost of development
Lower licensing fees to decrease development costs and ensure continued commitment to program success

2. Increase speed of development
Challenge traditional approaches through regulatory engagement

Streamline development through strategic partnerships and a platform approach to drug development

3. Enable the entire ecosystem
Provide expertise through in-house Brydge Solutions and leveraging the Odylia Board

Enable the entire ecosystem through Initiatives that impact the broader field

Odylia Therapeutics

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Join Paula to support Odylia Therapeutics

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Join Paula to support Odylia Therapeutics

Join Paula to support Odylia Therapeutics

Odylia Therapeutics

Donors

Become a supporter!

Become a supporter!

Turn this donation into a movement

Odylia Therapeutics

Odylia Therapeutics