Mechanism-first
grounded in disease biology
Vascular instability driven by pericyte dysfunction is increasingly recognised as a root cause of genetic blood vessel, cardiovascular, renal, ocular, and neurodegenerative diseases.
We have created the periSCOPE platform through our integrated relationship with LUMC and other collaborators. The platform supports broad therapeutic opportunities, our initial focus is on Hereditary Haemorrhagic Telangiectasia (HHT), an inherited rare genetic disorder affecting 1.4 million people worldwide.
While our proprietary periSCOPE platform supports broad therapeutic opportunities, our initial focus is on Hereditary Haemorrhagic Telangiectasia (HHT), an inherited rare genetic disorder affecting 1.4 million people worldwide.
We are translating clear links from HHT preclinical models to clinical endpoints and defining patient groups for trials.
grounded in disease biology
clear link from preclinical models to clinical endpoints
applicable across multiple vascular indications