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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Summer 2025 RFA: Personalized Approaches for Understanding, Assessing and Improving Gait in Parkinson’s Disease Research Program, 2026A Novel Digital Music-based Autonomous Personalized Walking Intervention to Improve Gait and Walking Automaticity in Parkinson Disease
Study Rationale:
People with Parkinson disease often take small, slow and unsteady steps, which makes it hard to get around and lowers their quality of life. While focusing on walking can help a little...
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Fall 2025 RFP: Data Advice To Action - DATA-PD, 2026Blood-based Signatures of CSF Synuclein SAA Positivity
Study Rationale:
The ability to identify people during life, who are likely to have underlying Lewy body pathology has been a game-changer. However, the current test (SAA) is limited...
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Research Grant, 2026From Functional Maps to Clinical Outcomes: Interpreting GBA1 Variant Effects in Parkinson's Disease
Study Rationale:
Genetic variants in the GBA1 gene are among the most important risk factors for Parkinson’s disease. GBA1 encodes an enzyme that breaks down waste inside lysosomes...
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Bridge Funding for Disrupted Neurodegenerative Research Grant Program, 2026Region-specific Effects of Pathology and Vocal Training
Study Rationale:
Voice and communication deficits are common in Parkinson’s disease. They occur early in the disease process, are progressive in nature, and significantly impact...
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Research Grant, 2026Disease Modeling for Neuronal Alpha-synuclein Diseases
Neuronal alpha-synuclein diseases (NSD), such as Parkinson’s disease, progress slowly and affect people differently, making it hard to predict when symptoms will appear or worsen. Current methods for...
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Summer 2023 RFP: Accelerating Biological Understanding and Therapeutic Translation for Parkinson’s Disease Program - Biology, 2026Characterization of Constrained Peptides Targeting LRRK2 and Downstream Signaling
Study Rationale:
Genetic mutations in LRRK2 are linked to familial Parkinson’s, however, there are currently no clinically approved inhibitors for LRRK2. In this study, we will...
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Our funding programs support basic, translational and clinical research from academia and industry.