CHANGING PEOPLE’S LIVES

Focusing on our goal to treat, and potentially cure, inherited diseases
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OUR PURPOSE

We believe it is essential to understand the people living with the genetic diseases that we are aiming to treat.

At PYC, we make it a priority to collaborate with patients and caregivers across our development process – to ensure that our RNA therapeutics best meet their needs.

We recognise the importance of developing therapies based on an understanding of both the disease and its broader impact on patients and their families.

Helpful resources for patients

Learn more about our disease areas.
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Retinitis Pigmentosa type 11 (RP11)

Learn about RP11 and the treatment we are developing for it.

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Autosomal Dominant Optic Atrophy (ADOA)

Learn about ADOA and the treatment we are developing for it.

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Phelan-McDermid Syndrome (PMS)

Learn about PMS and the treatment we are developing for it.

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Autosomal Dominant Polycystic Kidney Disease (ADPKD)

Learn about ADPKD and the treatment we are developing for it.

OUR PARTNERS

PYC is proud to partner with:

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