We are a clinical-stage biotech company with a purpose to discover and develop RNA therapies that change the lives of patients with genetic diseases.
Our RNA delivery platform technology offers the potential for safer and more effective treatment of the underlying cause of many inherited diseases. At PYC, we seek to treat the underlying cause of the genetic disease, not just the symptoms. Our proprietary RNA therapies aim to halt genetic disease progression and – in some cases – potentially reverse it.
We are currently developing a pipeline of novel therapies in clinical and pre-clinical stage programs, which are focused on diseases of the eye, the central nervous system and the kidney.
We recognise the urgent need to develop treatments for genetic diseases, many of which have no current treatment options available. By designing high-affinity carriers for RNA therapeutics that overcome the major limitations of current genetic treatments, we aim to accelerate treatment availability to patients. We are dedicated to developing exceptional, life-changing therapies.
Meet our global team of leading scientists, clinicians and industry professionals.