NLR-STRUCTURE

Drug Discovery Initiative for the Treatment of Chronic Inflammatory Disease

 Coordinatore ASTON UNIVERSITY 

 Organization address address: ASTON TRIANGLE
city: BIRMINGHAM
postcode: B4 7ET

contact info
Titolo: Prof.
Nome: Roslyn
Cognome: Bill
Email: send email
Telefono: +44 121 204 4274

 Nazionalità Coordinatore United Kingdom [UK]
 Totale costo 154˙617 €
 EC contributo 154˙617 €
 Programma FP7-PEOPLE
Specific programme "People" implementing the Seventh Framework Programme of the European Community for research, technological development and demonstration activities (2007 to 2013)
 Code Call FP7-PEOPLE-2013-IIF
 Funding Scheme MC-IIF
 Anno di inizio 2014
 Periodo (anno-mese-giorno) 2014-05-02   -   2015-05-01

 Partecipanti

# participant  country  role  EC contrib. [€] 
1    ASTON UNIVERSITY

 Organization address address: ASTON TRIANGLE
city: BIRMINGHAM
postcode: B4 7ET

contact info
Titolo: Prof.
Nome: Roslyn
Cognome: Bill
Email: send email
Telefono: +44 121 204 4274

UK (BIRMINGHAM) coordinator 154˙617.60

Mappa


 Word cloud

Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.

drug    chronic    diseases    structure    industry    discovery    market    disease    inflammatory    world    clinical    therapeutics    therapeutic    nlrp   

 Obiettivo del progetto (Objective)

'Chronic inflammation is central to disease progression and organ failure in the majority of common human diseases, including cardiovascular disease, inflammatory bowel disease, chronic kidney & liver disease, gout, asthma, arthritis and cancer. Together, these chronic conditions contribute substantially to morbidity and mortality and generate a profound socioeconomic burden. The NLRP-STRUCTURE project will pave the way for the development of first-in-class drugs that can target select NLRP inflammasome members within different diseases endemic to the EU population. World-leading protein expression technologies will be integrated with unique chemoproteomic drug discovery platforms with the purpose of achieving rationalized drug development. Structure-activity guided medicinal chemistry will allow the team to propose drug leads that can be used in the synthesis of a new generation of small molecule pharmaceuticals for chronic inflammatory disease management. The project can provide data and information sourced from health databases, basic and translational research, and in-house analysis by a network of academic/clinical/industry experts. Thus, NLRP-STRUCTURE has the potential to develop new diagnostic, prognostic and therapeutic strategies that will improve the clinical care of patients across a wide range of chronic and debilitating disease. The entry of pipeline molecules will boost the anti-inflammatory therapeutics industry, thereby bringing about further economic stimulation to the therapeutics market in the coming years. The research objectives of NLRP-STRUCTURE will position the Host and partners in positions as world leader, as an acknowledged centre of global excellence in NLRP therapeutic discovery. Integral to the proposal is the development of patent landscapes and strategic partnerships that will play substantial roles in shaping the market in the future.'

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