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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.

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

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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