Nurr1 as a Genetic Target for Treating Levodopa-induced Dyskinesias (LIDs) in Parkinson's Disease
Case ID:
TEC2014-0099
Web Published:
6/23/2016
Executive Summary
Patients afflicted with Parkinson’s disease often develop severely debilitating movement disorders as side effects from currently available treatment options. Researchers at MSU propose to use a new gene therapy approach that will both reduce these side effects and prolong the effectiveness of treatment by targeted gene silencing.
Description of Technology
L-Dopa induced dyskinesia (LID) is a side effect of prolonged chronic use of L-Dopa medication. A hyper-expression of Nurr1 protein in affected brain areas might underlie these side effects. Local injection of vectors encoding target genes in affected striatum can directly prevent the hyper-expression allowing for potentially improved fine-tuned response for motor control.
Key Benefits
- Improved quality of life for Parkinson’s patients
- Improved and prolonged benefit for movement disorders
Applications
- Treatment of LID in patients with Parkinson’s disease
- Potentially useful in the treatment of other movement disorders
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Patent Status:
US patent application published, no. 20170198295; foreign patent application published, no. WO2015188077A1
Licensing Rights Available
Full licensing rights available
Inventors: Fredric Manfredsson, Kathy Steece-Collier, Jack Lipton, Timothy Collier, Nicholas Kanaan, Caryl Sortwell
Tech ID: TEC2014-0099
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For Information, Contact:
Anupam Jhingran
Technology Manager
Michigan State University
jhingran@msu.edu