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Funded Studies

The Foundation supports research across basic, translational and clinical science to speed breakthroughs that can lead to the creation of new treatments and a better quality of life for people with Parkinson's disease.

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Previously funded studies appear chronologically, with the most recent appearing first.

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  • Priority Biology, 2021
    Developing New Therapeutic Drugs for Parkinson’s in Human Stem Cell Neurons

    Study Rationale:
    Neurons derived from stem cells from people with Parkinson’s disease offer an opportunity to perform drug and target discovery. We completed a screen of 4,000 drug compounds in such...

  • Therapeutic Pipeline Program, 2021
    Brain-penetrating Antisense Oligonucleotide to Down-regulate Alpha-synuclein

    Study Rationale:
    Antisense oligonucleotides (ASOs) are a new type of therapeutic that have promise for treating Parkinson’s disease. They act by modifying the production of specific proteins, such as...

  • Research Grant, 2020
    California Parkinson’s Disease Registry

    Study Rationale:    
    This project will support operations and enhancement of the California Parkinson’s Disease Registry (CPDR) for one year. CPDR captures and stores information on all Parkinson’s...

  • Priority Biology, 2020
    Effects of LRRK2 Variants on GCase Activity in iPSC-derived Dopamine Neurons and Microglia

    Study Rationale:
    There is contradictory evidence on whether the LRRK2 and GBA genes, and the proteins that they encode, interact in their effects on Parkinson’s disease. Some studies suggest that...

  • Research Grant, 2020
    Evaluation of ANAVEX2-73 (blarcamesine) in Participants with Parkinson’s Disease

    Study Rationale:    
    We are testing ANAVEX2-73 (also known as blarcamesine), which previous research has shown helps improve behaviors as well as normalizes biochemical changes in a Parkinson’s...

  • , 2020
    The Role of USP30 in Idiopathic Parkinson’s Disease

    Study Rationale:    
    Dopamine neurons are highly vulnerable to age-dependent increases in mitochondrial dysfunction, oxidative stress, and protein accumulation due to their high metabolic activity...

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