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 Objectives
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:
- Optimise 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.
- Analyse the IP position and strategy, as well as the market and (existing and emerging) competitors.
- 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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Vergelijkbare projecten uit andere regelingen
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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.
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