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PCSP

Odour-GPCRs based technology for detection and stratification of cancer: Prostate Cancer Smell Print as first vertical market

Total Cost €

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EC-Contrib. €

0

Partnership

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 PCSP project word cloud

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

ogpcr    trial    scalable    volatile    organic    print    cancer    identification    risky    penetration    born    positives    compounds    market    scenarios    readable    resembles    detection    assays    tested    financial    biotech    permits    ogpcrs    selling    initial    patients    difficult    pretends    receptors    negatives    showed    false    unnecessary    standard    analysed    patented    nose    antigen    universal    definition    percentage    quantify    broad    dog    care    recognition    amount    ed    signalling    activation    adoption    stress    prototype    prostate    expressing    detect    saving    technologies    cover    invasive    cascade    dogs    accurate    producing    appreciable    olfactory    feasibility    accuracy    samples    extension    clinical    screening    trained    technology    expression    pcsp    expertise    canvax    appropriate    transferring    detecting    physicians    discrimination    cells    validation    diagnosis    owns    subject    types    acquisition    pca    regulatory    anxiety    smell    ideal    coupling    urine    array    points    clinic    fluorescent    unmet    gain    heterologous    diagnostic   

Project "PCSP" data sheet

The following table provides information about the project.

Coordinator
CANVAX BIOTECH SL 

Organization address
address: POLIG TECNOCORDOBA CL 14 E PARC 47 PLANTA 2
city: CORDOBA
postcode: 14014
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 Spain [ES]
 Project website http://canvaxbiotech.com/canvax-is-awarded-with-phase-i-sme-instrument-h2020/
 Total cost 71˙429 €
 EC max contribution 50˙000 € (70%)
 Programme 1. H2020-EU.3.1.3. (Treating and managing disease)
 Code Call H2020-SMEINST-1-2014
 Funding Scheme SME-1
 Starting year 2015
 Duration (year-month-day) from 2015-05-01   to  2015-10-31

 Partnership

Take a look of project's partnership.

# participants  country  role  EC contrib. [€] 
1    CANVAX BIOTECH SL ES (CORDOBA) coordinator 50˙000.00

Map

 Project objective

PCSP project is born out of the unique expertise developed after years of R&D at Canvax Biotech, and aims at transferring a technology to cover an unmet clinical need, accurate diagnosis of prostate cancer (PCa). Canvax owns a unique set of patented technologies: i) high expression of olfactory receptors (oGPCRs) in heterologous cells, ii) coupling to a signalling cascade and iii) readable fluorescent assays to quantify oGPCR activation. Canvax is producing an array of cells expressing oGPCRs that could be used to detect several types of cancer, including PCa, by detecting cancer-associated volatile organic compounds in urine. The technology is currently being tested in a PCa clinical trial. PCa detection has been widely carried out using the prostate specific antigen test. However, its low accuracy resulted in a high percentage of false positives and a still appreciable amount of false negatives. Several recent studies showed that trained dogs could detect PCa from urine samples with the higher accuracy. However, the use of dogs in clinic is difficult and non-scalable. Canvax PCSP test resembles a dog nose that pretends to be a universal screening method for PCa-type discrimination identifying, in simple urine test, patients in need of further, more invasive diagnostic procedures with higher accuracy than current standard of care, saving stress, anxiety and unnecessary risky procedures. The easy use and low cost of this technology makes it ideal for broad adoption. Different scenarios have been described for market penetration and would be subject of the feasibility study during phase I: Smell print definition, regulatory and market permits acquisition, clinical trial design, identification of best-selling points, EU extension and financial costs will be analysed. The appropriate measures will be applied during phase II, together with prototype validation in a large clinical trial to gain recognition within the physicians, and initial exploitation of the technology

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

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