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MOOD

Feasibility Study for the introduction into pre-clinical study domain of the first-of-a-kind Multi Organ On Device (MOOD) technology

Total Cost €

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EC-Contrib. €

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Partnership

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Project "MOOD" data sheet

The following table provides information about the project.

Coordinator
REACT4LIFE SRL 

Organization address
address: VIA DOMENICO FIASELLA 1
city: GENOVA
postcode: 16121
website: n.a.

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 Italy [IT]
 Project website https://www.react4life.com/
 Total cost 71˙429 €
 EC max contribution 50˙000 € (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-2018-2020-1
 Funding Scheme SME-1
 Starting year 2018
 Duration (year-month-day) from 2018-08-01   to  2019-01-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    REACT4LIFE SRL IT (GENOVA) coordinator 50˙000.00

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 Project objective

Advances in molecular biology have significantly increased the understanding of the biology of different diseases. Nevertheless, these advances are not fully translated yet into improved treatments for patients, specifically for what pertains to the oncological disorders. One of main reasons for this shortcoming is the lack of reliable in vivo models that accurately predict drug efficacy and toxicity, so to translate these results from preclinical studies to the clinic. In present project we address the major challenge of the preclinical stage in drug development, by offering a proprietary Multi-Organ-On-Device (MOOD), being an advanced fluidic multi-chamber bioreactor, a 3D model of breast cancer tissue cultured onto a membrane mimicking the blood vessel barrier, which jointly reproduce the physio mimetic environment of the cancer disease. In this way, MOOD technology enables the execution of standard pre-clinical assays, such as tumor cell migration and intravasation, drug efficacy and toxicity assays, thus bypassing unreliable, costly and ethically relevant mice studies. The validation of the MOOD device paves the way for the replacement, reduction and refinement (3Rs) of animal studies on global scale, allowing for dramatic cost reduction in the pre-clinical stage and for accelerated time to market for pharmaceutical companies and CROs. The objectives of this feasibility study will be the deep understanding of the market and its technological and economic requirements, so to properly stream line the industrialization of MOOD platform. We expect our MOOD technology to exert a disruptively beneficial impact on drug development process and thus, human health and national economies.

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

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