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.

Subsidie
€ 150.000
2022

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:

  1. Optimize and subsequently test the technical feasibility of our two drug candidates in AD-like in vitro and in vivo models.
  2. Explore the commercial opportunity of our novel AD drugs.
  3. 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

Startdatum1-6-2022
Einddatum31-5-2024
Subsidiejaar2022

Partners & Locaties

Projectpartners

  • UNIVERSITA DEGLI STUDI DI VERONApenvoerder

Land(en)

Italy

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