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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. €

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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.

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

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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