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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, 2025
    Clinical Evaluation of 18F-FD4 as a Potential Alpha-synuclein PET Imaging Biomarker
  • Research Grant, 2025
    Applying the Neuronal Alpha-synuclein Disease Integrated Staging System in Multiple System Atrophy

    Study Rationale: The neuropathological hallmark feature of Parkinson’s disease (PD) is the accumulation of a misfolded protein called alpha-synuclein in neurons, which qualifies PD as a neuronal...

  • Research Grant, 2025
    Validation of the Usability of Patient-specific Midbrain Organoids for LRRK2 Drug Discovery in Parkinson’s Disease

    Study Rationale: Parkinson’s disease (PD) is a progressive brain disorder characterized by the loss of dopamine-producing neurons. OrganoTherapeutics has developed advanced midbrain organoid models...

  • Parkinson’s Disease Therapeutics Pipeline Program, 2025
    Isoform Specific Suppression of dIRE-SNCA with an ASO

    Study Rationale: Alpha-synuclein (SNCA) aggregation is a hallmark of Parkinson’s disease (PD). Rare SNCA genetic duplications and triplications cause early-onset PD, suggesting a link between SNCA...

  • Parkinson’s Disease Therapeutics Pipeline Program, 2025
    Next Generation Treg Therapy for Parkinson’s Disease

    Study Rationale: Parkinson’s disease (PD) occurs because of the degeneration of the neurons that produce the neurotransmitter dopamine. This causes the disease signs and symptoms. Nerve cell...

  • Parkinson’s Disease Therapeutics Pipeline Program, 2025
    Novel Small Molecules to Slow PD Progression in a Genetically Defined Subset of People with PD

    Study Rationale: Currently, drug discovery efforts for neurodegeneration are almost exclusively focused on disease risk, not the progression biology that afflicts patients when they present with...

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