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CHAMPION SIGNED

Cartilage Healing Approach Merging Polymer InnOvation with Nature

Total Cost €

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EC-Contrib. €

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Partnership

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 CHAMPION project word cloud

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

unlike    injury    prochondrogenic    resorbable    off    designed    injuries    time    elusive    shape    centres    patients    bone    afflicts    gelrinc    situ    cells    benefit    focal    microenvironment    excellence    chondrocytes    limiting    trials    joint    completing    gradually    implants    clinical    cartilage    symptomatic    biologicals    denatured    action    glycol    therapeutic    right    hyaline    frequent    optimizing    polyethylene    surgery    complexity    knee    procedure    mark    human    risks    arthroscopic    migration    inwards    commercialization    defect    mode    alternative    market    ultraviolet    annually    promise    outcome    barrier    entrance    defects    quick    implantation    light    differentiate    regulatory    failed    conforming    painful    million    microfracture    degradation    replacement    shelf    liquid    implant    articular    form    gained    cellular    optimal    marrow    re    pursuit    ce    synchronized    treatment    multiple    poor    total    limited    fibrinogen    successful    cured    stem    acellular    rate    ready    undesired    cell    replaced    body    longterm    preventing    channels    requiring    harnesses    interventions    treatments    resorbs    2017    stimulation    realized    outside    osteoarthritis   

Project "CHAMPION" data sheet

The following table provides information about the project.

Coordinator
REGENTIS BIOMATERIALS LTD 

Organization address
address: HA ILAN STREET 2 NORTHERN INDUSTRIAL ZONE
city: OR AKIVA
postcode: 30600
website: www.regentis.co.il

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 Israel [IL]
 Total cost 3˙121˙700 €
 EC max contribution 2˙185˙190 € (70%)
 Programme 1. H2020-EU.3. (PRIORITY 'Societal challenges)
2. H2020-EU.2.3. (INDUSTRIAL LEADERSHIP - Innovation In SMEs)
3. H2020-EU.2.1. (INDUSTRIAL LEADERSHIP - Leadership in enabling and industrial technologies)
 Code Call H2020-SMEInst-2018-2020-2
 Funding Scheme SME-2
 Starting year 2019
 Duration (year-month-day) from 2019-06-01   to  2021-05-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    REGENTIS BIOMATERIALS LTD IL (OR AKIVA) coordinator 2˙185˙190.00

Map

 Project objective

Cartilage injury afflicts over one million patients annually in Europe. Focal knee cartilage defects are as painful and limiting as osteoarthritis and can lead further degradation requiring total knee replacement surgery. Focal knee cartilage injuries are typically treated by bone marrow stimulation (Microfracture) which has limited benefit due to a high failure rate, poor longterm outcome and frequent required re-interventions. Alternative therapeutic products in the form of cellular/biologicals treatments have failed due to complexity and multiple surgery risks. With the promise of cell-based procedures not realized, the pursuit of an optimal treatment for symptomatic articular cartilage defects in the knee joint remains elusive. GelrinC is a simple, off-the-shelf treatment for focal injuries in the knee cartilage. It is a ready-to-use liquid cured in-situ by ultraviolet light to form a resorbable implant conforming to the shape and depth of the defect. Unlike other acellular implants, GelrinC was designed to support the formation of hyaline cartilage through a unique Mode-of-Action: Formation of a cell barrier thus preventing migration of undesired cells into the defect. At the same time, GelrinC harnesses the established prochondrogenic potential of polyethylene glycol, its major component, to provide the right microenvironment for the body’s own stem cells to differentiate into chondrocytes. Due to the presence of the denatured human fibrinogen in GelrinC, the implant resorbs from the outside inwards and thus is gradually replaced with new hyaline-like cartilage in a synchronized process. GelrinC gained a CE mark in 2017 and it is regulatory ready for commercialization in Europe. The next steps allowing quick, successful market entrance are optimizing the production process, completing a phase III clinical trials,improving the procedure towards arthroscopic implantation; and creating commercialization channels including centres of excellence in Europe.

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

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