Targetting neutrophil-mediated neurotoxicity for the treatment of Alzheimer's Disease
The NeutrAD project aims to develop and commercialize the first disease-modifying Alzheimer's drugs targeting neutrophil-mediated neurotoxicity, with promising results in preclinical models.
Projectdetails
Introduction
With the NeutrAD ERC PoC project, we present the first disease-modifying Alzheimer's Disease (AD) drugs that abrogate leukocyte-mediated neurotoxicity and represent a novel class of drugs in the treatment of AD.
Background
AD is a neurological disorder characterized by progressive deterioration of cognitive function and leads to death within 3-9 years after diagnosis. It is highly prevalent in the elderly, and it is estimated that 35 million patients suffer from the disease worldwide. As a result, AD has tremendous social and economic impact.
This situation is aggravated by the lack of disease-modifying drugs, as current therapies only provide short-term symptomatic benefit. Hence, novel therapeutic approaches are of critical importance to resolve this urgent and growing health crisis.
Novel Drug Candidates
Our novel anti-AD drug candidates use a neutrophil-targeted approach and unlock a new avenue for the millions that suffer from AD. Growing evidence supports the role of inflammation in the development of neurodegeneration in AD.
For example, our previous research has demonstrated a role for neutrophils in the induction of memory decline and neuropathological hallmarks of AD. Furthermore, our data shows that a highly activated and degranulating neutrophil phenotype induces neurotoxicity in an in vitro AD context. Preliminary results have also demonstrated that our novel drug candidates rescue neuronal death and have disease-modifying potential in AD-like mouse models.
Project Goals
In NeutrAD, we will explore the technical and commercial potential of our drug candidates as the first disease-modifying drugs against AD. Specifically, we will:
- Optimize and subsequently test the technical feasibility of our two drug candidates in AD-like in vitro and in vivo models.
- Explore the commercial opportunity of our novel AD drugs.
- Analyze the IP position and strategy, as well as the market and existing and emerging competitors.
Finally, we will consolidate the project outcomes in an investor-ready business plan.
Financiële details & Tijdlijn
Financiële details
Subsidiebedrag | € 150.000 |
Totale projectbegroting | € 150.000 |
Tijdlijn
Startdatum | 1-6-2022 |
Einddatum | 31-5-2024 |
Subsidiejaar | 2022 |
Partners & Locaties
Projectpartners
- UNIVERSITA DEGLI STUDI DI VERONApenvoerder
Land(en)
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Novel biomarkers for improving diagnostics, prognostics, and treatments of Alzheimer’s disease
ADVANCE-AD aims to enhance Alzheimer's diagnostics and treatment by developing cost-effective blood-based biomarkers and algorithms for early detection and intervention in pre-symptomatic patients.
Repurposing a human drug to treat Alzheimer’s disease
This project aims to validate an approved drug that inhibits tau accumulation in Alzheimer's, advancing it towards commercialization as a novel treatment for the disease.
Probing (Orphan) Nuclear Receptors in Neurodegeneration
NeuRoPROBE aims to develop chemical probes and PROTACs for orphan nuclear receptors TLX and Nurr1 using AI to advance therapeutic strategies against neurodegenerative diseases.
Deciphering Alzheimer’s disease molecular subtypes to advance treatment development.
This project aims to identify Alzheimer's disease subtypes through CSF proteomics to develop tailored treatments and theragnostic tools linked to cognitive decline and genetic factors.
Gamma-secretase allosteric modulation as preventive therapy in Alzheimer’s Disease
This project aims to validate gamma-secretase allosteric modulators as safe, effective, and affordable preventative treatments for Alzheimer's Disease using an innovative xenotransplantation model.
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ATI's AT-001 aims to stop and revert dementia by preventing protein aggregation, with promising Phase IIa results leading to upcoming registration trials and POC studies for commercialization.
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The project aims to develop a novel human brain-organoid model, called connectoids, to replace animal testing for Parkinson's disease, enhancing therapy monitoring and reducing societal burdens.
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