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UK funding (542 469 £) : United Kingdom Primary Sjogren's Syndrome Registry (UKPSSR) Ukri01/12/2008 UK Research and Innovation, Royaume Uni

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United Kingdom Primary Sjogren's Syndrome Registry (UKPSSR)

Abstract Primary Sjogren s syndrome (PSS) is a chronic condition that affect up to 3% of adults in the United Kingdom (UK). Although the commonest symptoms of PSS are dry eye, dry mouth, joint pain and profound fatigue, almost any part of the body can be affected. Moreover, PSS is associated with 40 times higher risk of developing lymphoma (a form of cancer). Patients with PSS also have poor quality of life and a significant proportion of PSS patients are unable to work because of their disease. Unfortunately, we know very little about what causes PSS and we have not found any effective treatment. However, several recent developments in PSS research have created a platform for finding new treatment for PSS and improving our understanding of the underlying disease processes of PSS. Firstly, the UK Sjogren?s Interest Group (UKSIG) have developed standardised methods to assess patients with PSS, so that we can test how good a specific treatment is and make comparison with other treatments. Secondly, a number of promising therapies for PSS have been developed in the last few years. Thirdly, emerging new research technologies offer new approaches in PSS research. The aim of this project is to capitalise on these recent developments by creating a database of 500 patients with PSS over a period of 3 years so that new treatments for PSS can be tested more quickly and efficiently and clinical studies can be carried out more effectively. We need so many patients because not all patients are suitable for all studies. We will assess the patients using the standardised methods mentioned earlier and blood samples from these patients will be stored for future research. Patients will be recruited from 24 hospitals across the UK and the assessment will be carried out at the local clinics. This is a UKSIG project, co-ordinated by doctors from Newcastle University, the Freeman Hospital and University Hospital of Birmingham. Many doctors involved in this project have participated in previous multi-centre studies organised by the UKSIG. The proposed database will provide a unique and valuable resource for clinical and academic studies as well as for identifying suitable patients for clinical trials. The database will make it quicker and easier to organise these studies. Furthermore, this project will encourage collaborative research between academia, National Health Service and industry, and will promote the use of standardised assessments in the management of patients with PSS.
Category Research Grant
Reference RCS G0800629
Status Closed
Funded period start 01/12/2008
Funded period end 30/03/2014
Funded value £542 469,00
Source https://gtr.ukri.org/projects?ref=G0800629

Participating Organisations

Newcastle University
HarmonicSS
University Hospitals Birmingham NHS Foundation Trust
University of Strasbourg
AbbVie Inc
University of Stavanger
Uppsala University Hospital
Nascient ltd
Queen Mary, University of London
The European League Against Rheumatism (EULAR)
University of Paris South 11
University of Liverpool
AstraZeneca plc
Novartis
National Institute of Health and Medical Research (INSERM)
Resolve Therapeutics, LLC
Northumbria University
University of Oxford
Great Western Hospitals NHS Foundation Trust
Uppsala University
ElectroCore LLC
Janssen Pharmaceutica NV
GlaxoSmithKline (GSK)
University of Glasgow
The Dudley Group NHS Foundation Trust
University of Leeds
The Binding Site
Erasmus MC
Oklahoma Medical Research Foundation (OMRF)
Columbia University Medical Center

Cette annonce se réfère à une date antérieure et ne reflète pas nécessairement l’état actuel. L’état actuel est présenté à la page suivante : University OF Newcastle Upon Tyne CHARITY, Newcastle upon Tyne, Royaume Uni.

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