Pipeline

Potential best-in-class therapies for neurodegenerative disorders

Potential
Indications
Program Mechanism of Action Discovery IND-enabling Clinical
Alzheimer’s disease KRSA-028 Anti-3pE amyloid beta mAb(THETA-enabled)    
Undisclosed Undisclosed Undisclosed    
Undisclosed Undisclosed Undisclosed    

3pE-Aβ = Amyloid beta with post-translational pyroglutamate modification (pE) at the 3rd amino acid position, which is enriched in AD amyloid plaques

The number of Americans with Alzheimer’s disease is projected to be around 13 million people by 2050, nearly double the number today. It is a disease with a massive and growing unmet need, with associated long-term healthcare costs projected to be over $1 trillion by 2050.

Despite the clear and significant burden, only two new disease-modifying therapies have been approved since 2003. Both are associated with high rates of amyloid-related imaging abnormalities (ARIA) and involve a high burden of care due to frequent intravenous infusions and MRI imaging. Moreover, multiple lines of evidence suggest these products do not maximize the efficacy achievable with this mechanism.

However, these first-generation therapies also validate the use of anti-amyloid-β antibodies as backbones to future, disease-modifying therapies in this indication. Together with our transferrin receptor (TfR)-based THETA technology, a well-established regulatory pathway, and an accelerated path to early proof of concept for both therapeutic activity and differentiation, Korsana is poised to rapidly develop the next generation of potentially best-in-class therapies for Alzheimer’s disease.

antibody imagery
KRSA-028 animated