Coordinatore | UNIVERSITY OF NEWCASTLE UPON TYNE
Organization address
address: Kensington Terrace 6 contact info |
Nazionalità Coordinatore | United Kingdom [UK] |
Totale costo | 7˙838˙853 € |
EC contributo | 5˙960˙532 € |
Programma | FP7-HEALTH
Specific Programme "Cooperation": Health |
Code Call | FP7-HEALTH-2013-INNOVATION-1 |
Funding Scheme | CP-FP |
Anno di inizio | 2013 |
Periodo (anno-mese-giorno) | 2013-10-01 - 2017-03-31 |
# | ||||
---|---|---|---|---|
1 |
UNIVERSITY OF NEWCASTLE UPON TYNE
Organization address
address: Kensington Terrace 6 contact info |
UK (NEWCASTLE UPON TYNE) | coordinator | 1˙452˙729.20 |
2 |
BIOMARIN NEDERLAND BV
Organization address
address: J H OORTWEG 21 contact info |
NL (LEIDEN) | participant | 1˙128˙014.00 |
3 |
ASSOCIATION INSTITUT DE MYOLOGIE
Organization address
address: BOULEVARD DE L HOPITAL 47-83 contact info |
FR (PARIS) | participant | 1˙044˙498.00 |
4 |
UNIVERSITY COLLEGE LONDON
Organization address
address: GOWER STREET contact info |
UK (LONDON) | participant | 591˙293.00 |
5 |
SCITO SA
Organization address
address: RUE DES HAIES 8 contact info |
FR (PARIS) | participant | 571˙266.80 |
6 |
ACADEMISCH ZIEKENHUIS LEIDEN
Organization address
address: Albinusdreef 2 contact info |
NL (LEIDEN) | participant | 531˙492.00 |
7 |
CONSULTANTS FOR RESEARCH IN IMAGING AND SPECTROSCOPY SCRL
Organization address
address: RUE LOUIS JAMME 24 contact info |
BE (LIEGE) | participant | 399˙800.00 |
8 |
KATHOLIEKE UNIVERSITEIT LEUVEN
Organization address
address: Oude Markt 13 contact info |
BE (LEUVEN) | participant | 120˙720.00 |
9 |
UNIVERSITA CATTOLICA DEL SACRO CUORE
Organization address
address: Largo Agostino Gemelli 1 contact info |
IT (MILANO) | participant | 120˙720.00 |
Esplora la "nuvola delle parole (Word Cloud) per avere un'idea di massima del progetto.
'BIOIMAGE-NMD will develop and apply imaging technology to monitor response to novel therapies in neuromuscular diseases (NMD) and will use Duchenne muscular dystrophy (DMD) as an exemplar disease. DMD is well characterised genetically and clinically but to date a disease modifying treatment is not available. One of the most promising developments for future treatment of NMD is RNA modulation through antisense oligonucleotides (AON). In DMD, AON are used for exon skipping and this is a genuine example of personalised medicine, where patients are treated according to their specific gene mutation. Quantitative Magnetic Resonance Imaging (MRI) and Magnetic Resonance Spectroscopic Imaging (MRSI) are used to assess structural and metabolic muscle pathology in NMD but their effectiveness in monitoring therapy is yet to be shown. The project will apply a simultaneous MRI/MRSI protocol in multi-centre clinical trials of AON therapy in DMD with the aim of establishing a clinical proof of principle that these imaging measures are effective biomarkers of therapeutic response. To enhance the imaging protocol, novel Diffusion Tensor MRI (DTI) methods will be developed and optimised to assess muscle microstructure and applied in these trials. The project will also develop methods for radiolabelling of AON and demonstrate the use of pre-clinical Positron Emission Tomography (PET)/MRI to assess the tissue targeting, bio-distribution and pharmacokinetics of AON in vivo. BIOIMAGE-NMD will deliver PET/MRI and MRI/MRSI technologies for both drug development and clinical evaluation roles which will significantly contribute to bringing personalized therapeutic interventions in rare and common diseases to the market.'
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