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FluAttack SIGNED

Validation of a novel antiviral drug candidate against influenza

Total Cost €

0

EC-Contrib. €

0

Partnership

0

Views

0

 FluAttack project word cloud

Explore the words cloud of the FluAttack project. It provides you a very rough idea of what is the project "FluAttack" about.

human    pathogens    options    urgently    organization    replication    lab    commercial    pandemic    characterise    actually    pandemics    function    virus    vivo    drug    hits    approved    start    strategy    agree    world    molecule    time    ic50    context    million    burden    patent    demand    molecules    creation    cells    preventing    went    solution    clinical    risk    infection    trials    mouse    advantage    data    powerful    antivir    few    perfect    anti    resistance    epithelial    societies    ipr    efficacy    extremely    economic    deaths    treat    stg    650    cellular    limited    viral    airway    health    repurposing    devastating    lt    validate    screening    reduce    solutions    with    therapeutic    infections    mode    viruses    specialists    limitations    secure    lives    potent    cancer    worldwide    respect    100nm    poc    compounds    family    heavy    innovative    preclinical    influenza    prevent    vaccination    predicted    action    hit    candidate    3d    agent    licensing    escape    rely    plan    erc    tests    severe    model    inhibitors   

Project "FluAttack" data sheet

The following table provides information about the project.

Coordinator
INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE 

Organization address
address: RUE DE TOLBIAC 101
city: PARIS
postcode: 75654
website: www.inserm.fr

contact info
title: n.a.
name: n.a.
surname: n.a.
function: n.a.
email: n.a.
telephone: n.a.
fax: n.a.

 Coordinator Country France [FR]
 Total cost 0 €
 EC max contribution 150˙000 € (0%)
 Programme 1. H2020-EU.1.1. (EXCELLENT SCIENCE - European Research Council (ERC))
 Code Call ERC-2019-PoC
 Funding Scheme ERC-POC-LS
 Starting year 2020
 Duration (year-month-day) from 2020-04-01   to  2021-09-30

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    INSTITUT NATIONAL DE LA SANTE ET DE LA RECHERCHE MEDICALE FR (PARIS) coordinator 139˙081.00
2    CNRS INNOVATION FR (PARIS) participant 10˙919.00

Map

 Project objective

With 3 to 5 million severe cases and up to 650,000 deaths per year worldwide, influenza viruses are not only major human pathogens, they are also a heavy economic burden to our societies. In addition, influenza pandemics can occur at any time with potential devastating effects in terms of lives and costs. Solutions to prevent infection, to treat severe influenza cases and to respond to a severe pandemic are currently extremely limited and rely on vaccination and on only few approved molecules. All these solutions have their limitations with respect to efficacy and all face the problem of viral resistance. Thus, the demand for new options against influenza infections is high. The World Health Organization (WHO) and influenza virus specialists agree that innovative and effective anti-influenza compounds with a reduced risk of viral escape are urgently needed. The main goal of this ERC PoC is to provide key data on a promising innovative therapeutic solution identified in the lab. Taking advantage of a powerful screening system we have developed during the ERC StG ANTIViR, we have identified a family of molecules as potent inhibitors of influenza virus (with IC50<100nM). The mode of action of these molecules is known and they actually target a cellular function essential to all influenza viruses. Preventing viral replication by targeting a cellular function is a novel approach, predicted to strongly reduce the risk of drug resistance. Importantly, one of our hits went through several phase II and III clinical trials as an anti-cancer agent, making this molecule a perfect candidate for drug repurposing. In this context, the specific objectives of this ERC PoC are: i) to further characterise and validate our best hit, in particular in commercial 3D human airway epithelial cells and in vivo in a mouse model, and ii) to secure IPR and to establish an exploitation strategy plan (patent licensing or creation of a start-up) to support future development and preclinical tests.

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The information about "FLUATTACK" are provided by the European Opendata Portal: CORDIS opendata.

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