Skip to main content
European Commission logo
italiano italiano
CORDIS - Risultati della ricerca dell’UE
CORDIS
CORDIS Web 30th anniversary CORDIS Web 30th anniversary

Innovative Glycan-based analysis for Cancer diagnostics

Descrizione del progetto

Sensibilità diagnostica per il cancro alla prostata

L’antigene prostatico specifico (PSA) è attualmente utilizzato come biomarcatore per il cancro alla prostata. Tuttavia, gli esami del PSA difettano di precisione diagnostica poiché presentano un alto tasso di falsi positivi, portando a trattamenti sbagliati e a biopsie prostatiche non necessarie. Per affrontare questo problema, gli scienziati del progetto GlyCan, finanziato dall’UE, hanno realizzato un esame diagnostico innovativo, in grado di rilevare i cambiamenti nei glicani nella proteina del PSA. Questo esame vanta una precisione dell’86 % e riesce a distinguere le forme sane da quelle anormali della proteina. L’approccio proposto dal progetto GlyCan mette a disposizione un metodo affidabile per l’analisi di biomolecole complesse, utilizzabile anche per altre malattie.

Obiettivo

Worldwide, there are 1.6M new prostate cancer (PCa) cases with 366k deaths annually. Novel PCa biomarkers are needed since the best current PCa biomarker (prostate specific antigen (PSA)) lacks PCa diagnostic accuracy often resulting in mistreatment of PCa patients. The false-positive rate of PSA in blood serum is ~75%. PSA test is applied together with digital rectal examination (DRE) for preliminary screening. If the combined results are suspicious, the patients undergo a biopsy to confirm PCa. Yet, there are 74% of needless biopsies representing a significant pain for PCa patients and societal/economic burden.

Based on a great commercial outcome from the ERC grant (311532) granted to Dr. Jan Tkac (co-founder/CSO of Glycanostics), the company has developed an innovative, non-invasive, early PCa diagnostics using blood serum. Instead of quantifying PSA, the innovative PCa diagnostic assay detect glycan changes on PSA protein (it discriminates between “healthy” PSA and “sick” PSA and accurately quantify the clinically relevant “sick” PSA). The technology is covered by two EPO patent applications owned by the company. The PCa diagnostic test with 95% accuracy will be applied as a 2nd opinion test in case of suspicious results from PSA & DRE examinations prior sending to a biopsy. PCa DX kit will be launched for clinics/hospital & cancer centres (B2B) and Prostate check home test for user-friendly application at homes (B2C).

Our PCa diagnostic technology is unique compared to our competitors focusing on analysis of other complex biomolecules such as a level of proteins, mRNA and circulating DNA. Moreover, we have competitive advantage over competitors in terms of cost per sample, assay accuracy, simplicity of the assay enabling the home testing and high-throughput.

Glycanostics consists of 7 core team members, 4 business and 4 scientific advisors making a great and highly experienced team that will bring these innovative PCa early diagnostic products to the market.

Invito a presentare proposte

H2020-EIC-SMEInst-2018-2020

Vedi altri progetti per questo bando

Bando secondario

H2020-SMEInst-2018-2020-1

Meccanismo di finanziamento

SME-1 - SME instrument phase 1

Coordinatore

GLYCANOSTICS SRO
Contribution nette de l'UE
€ 50 000,00
Indirizzo
KUDLAKOVA 1848/7
841 01 Bratislava
Slovacchia

Mostra sulla mappa

PMI

L’organizzazione si è definita una PMI (piccola e media impresa) al momento della firma dell’accordo di sovvenzione.

Regione
Slovensko Bratislavský kraj Bratislavský kraj
Tipo di attività
Private for-profit entities (excluding Higher or Secondary Education Establishments)
Collegamenti
Costo totale
€ 71 429,00