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NeutroCure SIGNED

Development of “smart” amplifiers of reactive oxygen species specific to aberrant polymorphonuclear neutrophils for treatment of inflammatory and autoimmune diseases, cancer and myeloablation.

Total Cost €

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EC-Contrib. €

0

Partnership

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 NeutroCure project word cloud

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

space    breakthrough    nature    treatment    haematopoiesis    tissues    signaling    previously    solutions    consists    causes    pharmaceutical    damaging    concentration    drugs    first    multiple    occurs    ros    drug    boosting    paradox    killing    safe    reverse    inflammation    pathological    extracellular    precise    settings    reactive    autoimmunity    commercialization    neutrocure    redox    organism    sme    cells    contributes    solution    abnormal    amplifiers    traps    species    attempt    patient    caused    academic    functions    trigger    severe    healthy    myeloablation    radio    resolution    cell    disturbance    uncontrolled    chemotherapy    nets    positive    inhibits    prodrug    despite    mechanisms    regulation    possibilities    realized    society    cancer    leads    clinical    proximal    cure    time    neutrophil    spatial    dysregulated    pathologic    activation    generation    neutrophils    modulation    aberrant    innovative    temporal    polymorphonuclear    normal    unexplored    oxygen    relieve    phenotype    deactivation   

Project "NeutroCure" data sheet

The following table provides information about the project.

Coordinator
FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN NUERNBERG 

Organization address
address: SCHLOSSPLATZ 4
city: ERLANGEN
postcode: 91054
website: www.uni-erlangen.de

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 Germany [DE]
 Total cost 2˙999˙998 €
 EC max contribution 2˙999˙998 € (100%)
 Programme 1. H2020-EU.1.2.1. (FET Open)
 Code Call H2020-FETOPEN-2018-2019-2020-01
 Funding Scheme RIA
 Starting year 2020
 Duration (year-month-day) from 2020-01-01   to  2024-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    FRIEDRICH-ALEXANDER-UNIVERSITAET ERLANGEN NUERNBERG DE (ERLANGEN) coordinator 629˙000.00
2    UNIVERSITATSKLINIKUM ERLANGEN DE (ERLANGEN) participant 640˙000.00
3    UNIVERSITY OF SURREY UK (GUILDFORD) participant 410˙998.00
4    CENTRO NACIONAL DE INVESTIGACIONESCARDIOVASCULARES CARLOS III (F.S.P.) ES (MADRID) participant 400˙000.00
5    LVIVSKYI NATIONALNYI MEDYCHNYI UNIVERSYTET IMENI DANYLA HALYTSKOHO UA (LVIV) participant 400˙000.00
6    REDOXIS AB SE (LUND) participant 400˙000.00
7    INSTITUT GUSTAVE ROUSSY FR (VILLEJUIF) participant 120˙000.00

Map

 Project objective

Reactive oxygen species (ROS) have key functions in healthy organism such as redox signaling for regulation of cell growth, triggering formation of neutrophil extracellular traps (NETs), and modulation of inflammation. Since in high concentration ROS are damaging to tissues, nature has evolved precise mechanisms to control their generation at the required time, concentration and space, proximal to their target. Disturbance of these mechanisms leads to aberrant ROS production that causes uncontrolled inflammation, occurs in myeloablation caused by radio- or chemotherapy and is a crucial feature of cancer cell phenotype as well as autoimmunity. Despite the damaging properties of ROS it is a paradox that pharmaceutical ROS amplifiers can reverse (“cure”) many pathologic features. For example, ROS-induced cancer cell killing inhibits cancer growth, ROS-induced deactivation of T-cells and NETs generation contributes to resolution of inflammation, and ROS-induced boosting of haematopoiesis can relieve myeloablation. These exciting possibilities have not been realized in clinical settings yet, since the high level of temporal and spatial control of ROS generation, required to allow for safe patient treatment, has yet not been achieved for any known drug. NeutroCure will be the first attempt to achieve a breakthrough solution to this problem. Using an innovative approach based on the multiple-trigger prodrug activation, this consortium will develop safe ROS amplifiers capable of boosting ROS specifically in abnormal polymorphonuclear neutrophils associated with cancer, uncontrolled inflammation and relevant for myeloablation without affecting normal cells. NeutroCure consists of 6 European academic partners and an SME who will promote commercialization of the new drugs. We expect that this project will have a great positive impact on the Society by providing previously unexplored treatment solutions for severe pathological conditions caused by dysregulated ROS-production.

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

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