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RAPID

The first effective remedy for acute pancreatitis disease

Total Cost €

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EC-Contrib. €

0

Partnership

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 RAPID project word cloud

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

capacity    clinical    validate    molecules    dossier    rapid    company    care    tubular    market    people    preclinically    yearly    tech    reinvested    drug    phases    endoscopic    ema    regulatory    orientale    university    spin    intensive    initiation    solution    disease    pharma    ap    position    complete    operated    admitted    diseases    off    dystrophy    ions    acute    rare    39    hospitalizations    burden    advantage    patients    finance    providers    ready    national    calcium    small    patented    frequent    trigger    muscular    overload    data    hyper    frame    license    prepare    therapeutic    emergency    prior    gastroenterology    duchenne    aggregate    plan    store    undergo    modulate    2024    visits    room    surgical    trials    healthcare    cluster    breakthrough    activation    pave    validation    orphan    diagnosis    candidate    globally    time    services    piemonte    indications    cellular    optimal    fda    utmost    pharmacological    innovation    preclinical    entry    designation    health    chemicare    myopathy    discharge    generating    accelerated    revenues    therapies    proved    pancreatitis    last    costing    million    solutions    paths   

Project "RAPID" data sheet

The following table provides information about the project.

Coordinator
CHEMICARE SARL 

Organization address
address: VIA AMICO CANOBIO 4/6
city: NOVARA
postcode: 28100
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.chemicare.it/
 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 2019
 Duration (year-month-day) from 2019-05-01   to  2019-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CHEMICARE SARL IT (NOVARA) coordinator 50˙000.00

Map

 Project objective

ChemICare is a high-tech spin-off of the University of Piemonte Orientale and has patented and preclinically developed small molecules that are unique in their capacity to modulate calcium ions uptake in cellular processes. Calcium overload associated with Store-Operated Calcium Entry hyper-activation has been proved to be to be the key trigger in a cluster of diseases, including Acute Pancreatitis, which affects over 10 million people globally and is the most common gastroenterology discharge diagnosis in Europe and the US. AP is associated with significant disease burden, emergency room visits, frequent hospitalizations, and patients often undergo endoscopic and surgical procedures and are admitted to intensive care, costing more than 20 B€ yearly to National Healthcare Services. Preclinical data obtained so far demonstrate that drug candidate 39 represents a breakthrough innovation in the field of pharmacological therapies for AP. We are now in the process of generating the last data to complete the preclinical regulatory dossier, which will pave the way for the Phase I and II clinical trials which will lead to an out-license agreement to a large pharma company prior to the initiation of Phase III. The revenues will therefore be reinvested to finance development of the same technology for other therapeutic indications associated with calcium overload (e.g. Duchenne Muscular Dystrophy and Tubular Aggregate Myopathy). This Phase 1 is of utmost importance to validate the market position of ChemICare molecules, apply for orphan designation, and plan the preclinical study necessary to prepare the clinical validation Phases in the frame of the Phase 2. Our goal is to have a solution ready for the market by 2024, which will be cost-effective for health providers and deliver optimal care to patients with AP. Such rapid time-to-market is possible because both EMA and FDA have accelerated paths for rare disease solutions that we will take advantage of.

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

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