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RESHAPE SIGNED

Reshaping undesired Inflammation in challenged Tissue Homeostasis by Next-Generation regulatory T cell (Treg) Approaches – from Advanced Technology Developments to First-in-Human Trials

Total Cost €

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EC-Contrib. €

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Partnership

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 RESHAPE project word cloud

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

biotech    cell    atmp    diseases    entities    backgrounds    undesired    presently    members    accompanied    supports    vitro    human    hsc    overcome    adoptive    imbalance    fih    transplantation    health    recipient    immune    gene    hematopoietic    biomarker    data    cells    generation    1st    clinical    limitations    inflammation    transfer    overcoming    basic    performed    translation    conditioning    immunity    medicinal    allotransplantation    preclinical    transform    transplant    studies    therapeutic    suffering    treatment    game    record    specificity    cas9    stem    graft    crispr    curative    functional    therapy    options    disease    broad    reaction    proven    stability    combat    technologies    antigen    care    vivo    science    host    encouraging    treg    allografts    option    tested    enhanced    pioneers    platforms    academic    economic    trials    patients    organ    limited    regenerative    function    longtrack    rejection    regulatory    triple    changer    models    reshape    medicine    ec    first    transdisciplinarity    versus    tissue   

Project "RESHAPE" data sheet

The following table provides information about the project.

Coordinator
CHARITE - UNIVERSITAETSMEDIZIN BERLIN 

Organization address
address: Chariteplatz 1
city: BERLIN
postcode: 10117
website: www.charite.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 13˙137˙396 €
 EC max contribution 13˙137˙396 € (100%)
 Programme 1. H2020-EU.3.1.3. (Treating and managing disease)
 Code Call H2020-SC1-2018-Single-Stage-RTD
 Funding Scheme RIA
 Starting year 2019
 Duration (year-month-day) from 2019-01-01   to  2022-12-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CHARITE - UNIVERSITAETSMEDIZIN BERLIN DE (BERLIN) coordinator 4˙137˙775.00
2    CENTRE HOSPITALIER UNIVERSITAIRE DE NANTES FR (NANTES) participant 2˙023˙468.00
3    THE CHANCELLOR, MASTERS AND SCHOLARS OF THE UNIVERSITY OF OXFORD UK (OXFORD) participant 1˙998˙550.00
4    MEDIZINISCHE HOCHSCHULE HANNOVER DE (HANNOVER) participant 1˙548˙050.00
5    TISSUSE GMBH DE (BERLIN) participant 1˙026˙250.00
6    CELL THERAPY CATAPULT LIMITED UK (LONDON) participant 975˙625.00
7    TXCELL FR (VALBONNE) participant 502˙077.00
8    NATURWISSENSCHAFTLICHES UND MEDIZINISCHES INSTITUT AN DER UNIVERSITAET TUEBINGEN DE (REUTLINGEN) participant 499˙500.00
9    INNOVATION ACTA S.R.L. IT (ROMA) participant 426˙100.00

Map

 Project objective

Adoptive transfer of regulatory T cells (Treg) is a promising new therapeutic option to reshape undesired intra-tissue immune imbalance in immune-related disease entities. It supports long-term function of allografts and use of Advanced Therapy Medicinal Products (ATMP) by overcoming the challenge of unwanted immune reaction by the recipient of the ATMP. Therefore, adoptive Treg therapy is a potential game changer in health care, particularly in immune diseases, organ & hematopoietic stem cell (HSC) transplantation, and regenerative medicine, including gene therapy. Based on the Triple-T concept - Transdisciplinarity, Technology, Translation - the major goal of RESHAPE is to transform the treatment of patients suffering from undesired immunity/inflammation, who presently have limited curative treatment options, by applying novel Treg approaches that overcome the limitations of 1st generation Treg product developments. Members of the consortium, with academic & biotech backgrounds, are pioneers in the development of Treg therapy from basic science to very recent encouraging First-In-Human (FIH) clinical trials of the 1st generation Treg products. They have a longtrack record of collaboration, including in EC-funded projects. The first clinical trials were performed to combat organ transplant rejection and Graft-versus-Host-Disease. However, promising preclinical studies offer a broad application field of Treg therapy beyond allotransplantation. Based on our preclinical & clinical data, we have identified several opportunities for improving Treg therapy, such as enhanced antigen specificity & functional stability, and recipient conditioning, that will be addressed by RESHAPE. The next-generation Treg products, developed by advanced technologies including CRISPR/Cas9, will be tested on platforms applying new methods for cell characteristics in both in vivo /in vitro models, and finally proven in FIH-clinical trials accompanied by biomarker and health economic studies

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

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