Small Molecule Inhibitors for Treating Demyelinating Diseases
Small molecules, targeting HDAC3, enhance myelin repair in demyelinating diseases and injuries
Technology Overview
Treatment with small-molecules targeting Histone Deacetylase 3 (HDAC3) can enhance re-myelination and functional nerve recovery in the central and peripheral nerve systems (CNS and PNS) in animal models of multiple sclerosis and peripheral neuropathy. Targeting HDAC3 with these inhibitors also rejuvenates the age-related decline in functional recovery after injury.
Applications
- Inhibiting histone deacetylase 3 may be used to treat demyelinating diseases.
- Histone deacetylase 3 inhibitors promote myelin repair and nerve regeneration after injury.
Market Overview
The most common demyelinating disease is Multiple Sclerosis (MS). More than 2.3 million people worldwide are affected by MS. Other myelination related neural disorders include Alzheimer’s disease, Parkinson’s disease, Huntington disease, and amyotrophic lateral sclerosis (ALS).
Investigator Overview
Qing (Richard) Lu, PhD., Division of Experimental Hematology and Cancer Biology
Technology ID
2017-0502
Business Opportunity
Exclusive License or Sponsored Research
Technology Type
Small Molecule
Stage of Development
Pre-Clinical - In Vivo
Patent Information
PCT Filed