Profile
We are developing a first-in-class therapeutic approach for Parkinson’s disease (PD) based on Catalytides, catalytic peptides, capable of degrading pathogenic protein aggregates.
Our lead program focuses on α-synuclein-targeting Catalytides, where we have already demonstrated in vivo efficacy, including disease-relevant functional improvements and reduction of pathological burden in PD models.
Highlights of α-Syn Catalytide
Identified effective sequences of Catalytide for α-Syn
Confirmed the efficacy in a mouse model of PD
Evaluated CNS drug delivery via nasal administration in mice and monkey
Confirmed reduced p-α-Syn positive aggregates in PD brain specimens treated with Catalytides (in vitro)
No adverse effects observed following two-week nasal administration in mice
In parallel, we are expanding our platform toward other neurodegenerative targets (Amyloid-beta, tau, TDP-43, SOD1).
Our Catalytide platform combines:
Identification of aggregation-prone core regions
Rational peptide design with catalytic activity
Pharmacological validation in disease models
We are actively seeking:
Collaborative research partners (PD models, biomarker evaluation, DDS)
We particularly welcome partnerships with companies and groups working on Parkinson’s disease and other neurodegenerative diseases such as AD etc., protein aggregation therapeutics.
Keywords
Parkinson’s disease / α-synuclein / Catalytic peptide / Protein aggregation / Neurodegeneration / Drug discovery / Licensing / Collaboration
We are developing a catalytic peptide (Catalytide) that degrades α-synuclein for the treatment of Parkinson’s disease.
We are seeking partners for collaboration, licensing-out, and co-development this program toward clinical application.