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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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  • Research Grant, 2019
    Astrocyte Activation as a Novel Marker of Disease Progression in Parkinson’s Disease: A PET Imaging Study

    Study Rationale:
    Brain inflammation, regulated by cells called microglia and astrocytes, has been shown to play a role in the initiation and progression of Parkinson’s disease. However, the role of...

  • Target Advancement Program, 2019
    Connexins as a New Therapeutic Target to Impede Spreading of Alpha-synuclein Pathology

    Study Rationale:
    Direct cellular connectivity has recently been implicated in the transfer of alpha-synuclein pathology associated with Parkinson’s disease. The gap junction proteins known as...

  • Therapeutic Pipeline Program, 2019
    Oligomeric Alpha-synuclein-specific Antibody-based Gene Therapy

    Study Rationale:
    Alpha-synuclein is the primary component of Lewy bodies, the hallmark of Parkinson’s disease (PD). In particular, soluble aggregates of alpha-synuclein, also referred to as oligomers...

  • Therapeutic Pipeline Program, 2019
    Study of a Levodopa Adjunctive Therapeutic without Dyskinesia Liability

    Study Rationale:
    Evidence suggests that levodopa’s efficacy and side effects (uncontrolled movements called dyskinesia) are caused by activating dopamine D1 receptors. An optimal Parkinson’s disease...

  • Research Grant, 2019
    Patient Reports on Cannabis Use in Parkinson's Disease

    Study Rationale:
    Medical marijuana (cannabis) is now legal in 47 states, and recreational use is legal in nine. Interest in cannabis for treating Parkinson’s disease (PD) is rapidly increasing...

  • Target Advancement Program, 2021
    Validating Genetic Modifiers that Affect Disease Onset in People with LRRK2 Mutations

    Study Rationale:
    Mutations in the LRRK2 gene are a genetic cause of Parkinson’s disease (PD). However, the disease risk for carriers of LRRK2 mutations varies widely. Other genes — or genetic...

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