This programme funds preclinical and clinical research focused on slowing, stopping, or reversing Parkinson’s. We do not fund research which is directed at symptomatic relief.Our grant funding process has changed! Due to the discontinuation of Grant Tracker, we will be returning to manual processes for research grant funding submissions. Please review all the guidance below for information on how to apply.Our funding remit
For preclinical research, we fund grants up to £250,000 (GBP) and prioritise projects that are likely to lead to clinical trials in people with Parkinson’s within 5 years. For clinical research, we fund clinical trials and sub-studies of trials in people with Parkinson’s. The grant amount is flexible but please contact us ahead of submission if you are thinking of applying for a clinical trial.
We fund internationally and accept applications from academics and commercial entities. However, the costs in commercial applications should be justified and equivalent to academic costs where possible.
How to apply for funding
Stage 1 applications should be submitted via email to research@cureparkinsons.org.uk.
All stage 1 application documents can be accessed at the bottom of this page, including:
Additional documents that can be included at this stage but are not mandatory and should be provided in their own format:
Following Research Committee review of stage 1 applications, stage 2 applications will be invited on an individual basis and provided with the necessary documents via email.
The application process
Please review the guidance for applicants document below for more information about how to apply and the application and review process. If you have any questions regarding our funding scope, application process or subsequent work with successful applicants, please email the Research Team. Thank you.
Cure Parkinson’s funds only projects with credible disease-modifying potential.
Successful proposals:
Demonstrate mechanisms that could protect or restore dopaminergic neurons
Show modulation of pathways clearly linked to PD progression (e.g., α-synuclein, mitochondrial dysfunction, LRRK2, neuroinflammation, autophagy-lysosomal pathways)
Aim to slow progression, not reduce symptoms
Predictor: If the project is symptomatic-only, it will not be funded.
Reviewers prioritize:
Proposals with a defined path to clinical trials
Studies that will produce data enabling IND-enabling steps or early-phase trials
High potential to rapidly move from bench → clinic
Partnerships with clinicians, trialists, or pharma/biotech
Predictor: High translational readiness is key.
Because Cure Parkinson’s leads global drug repurposing efforts, high-scoring projects often:
Test already-approved drugs with plausible mechanisms for PD
Use computational, epidemiological, or mechanistic evidence supporting repurposing
Leverage safety data from other indications
Predictor: Repurposing proposals are often prioritized.
Competitive proposals include:
Mechanistic pilot studies
Preclinical efficacy in at least one PD model
Target validation evidence
Feasibility data for biomarkers or assays
Especially important for high-risk or novel mechanisms.
Predictor: Demonstrated feasibility increases confidence.
Cure Parkinson’s requires:
PD-relevant models (α-synuclein models, LRRK2, PINK1/Parkin, toxin models, iPSC-derived neurons)
Replication across more than one model if possible
Appropriate controls and rigorous experimental design
Predictor: Translatable, physiologically relevant models strongly impact scores.
Strong applications demonstrate:
Clear objectives over 12–36 months
Quantifiable milestones
Go/no-go decision points
Risk-mitigation strategies
Realistic budget and timelines
Predictor: Clarity and feasibility significantly matter.
Reviewers expect:
Expertise in PD biology and translational neuroscience
Team members with drug development or clinical trial experience
Access to specialized laboratory, imaging, and clinical infrastructure
A collaborative multidisciplinary approach
Predictor: Credible team with the capacity to deliver.
Favorable topics include:
α-synuclein aggregation/spread
Neuroinflammation and microglial activation
Mitochondrial dysfunction
Oxidative stress pathways
Lysosomal/autophagy defects
Gut–brain axis mechanisms
LRRK2, GBA, and related genetic pathways
Predictor: Mechanistic relevance to PD progression.
Cure Parkinson’s values biomarker development for:
Patient stratification
Target engagement
Progression measurement
Outcome sensitivity
Biomarker-ready proposals score higher.
| Pitfall | Why It Hurts |
|---|---|
| Symptomatic treatment (not disease-modifying) | Mission misalignment |
| Weak translational plan | Low probability of real-world impact |
| Insufficient preliminary data | High scientific risk |
| Poorly justified mechanism | Weak biological plausibility |
| Use of irrelevant or low-quality models | Low confidence in results |
| Overly ambitious design for short-term funding | Feasibility concerns |
| No biomarker strategy | Missing translational components |
| Lack of expertise in drug development or clinical translation | Execution risk |
This programme funds preclinical and clinical research focused on slowing, stopping, or reversing Parkinson’s.
Sponsor Institute/Organizations: Cure Parkinsons Trust
Sponsor Type: Corporate/Non-Profit
Address: 120 New Cavendish Street, London, W1W 6XX
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12-Jan-2026 , 13-Apr-2026 , 22-Jun-2026 , 12-Oct-2026
$332,500
Affiliation: Cure Parkinsons Trust
Address: 120 New Cavendish Street, London, W1W 6XX
Website URL: https://cureparkinsons.org.uk/research/for-researchers/apply-for-funding/quarterly-research-grant/
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