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OxThera coordonne le projet Elimox du 7e PC - 2,19 millions EUR dédiés au développement d'un médicament pour traiter l'hyperoxalurie
Date:9/24/2013

;Recherche au profit de groupes particuliers - Recherche au profit des PME ». Le consortium comprend les 12 partenaires suivants : OxThera AB (Suède), Cobra Biologics Ltd (Royaume-Uni), SymbioPharm GmbH (Allemagne), Ergomed Clinical Research Ltd (Royaume-Uni), Universitätsklinikum Bonn (Allemagne), Hospices civils de Lyon (France), University College London Hospitals NHS Foundation Trust (Royaume-Uni), Galenica AB (Suède), K.A.B.S. Laboratories Inc. (Canada), Medizinisches Versorgumszentrum Institute für Microökologie (Allemagne), TNO (Pays-Bas) et Bio-Images Research Ltd (Royaume-Uni).

À propos de l'hyperoxalurie primaire

L'hyperoxalurie primaire est un trouble génétique autosomal inné rare qui conduit à des élévations marquées des taux d'oxalate endogène dans le plasma et l'urine. Il existe un grand besoin médical insatisfait en termes de traitements efficaces de l'hyperoxalurie. Le seul remède disponible actuellement est la greffe combinée de foie et de rein.

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Cette étude a été financée par le septième programme-cadre de l'Union européenne géré par l'Agence exécutive pour la recherche (AER) http://ec.europa.eu/research/rea (FP7/2007-2013) dans le cadre de la convention de subvention no FP7-SME-2013.

Il n'existe aucun accord commercial anticipé susceptible d'imposer des limites à l'exploitation, aux informations ou aux inventions ultérieures générées par ce projet.

Pour tout complément d'information, veuillez contacter :

Elisabeth Lindner, coordinatrice du projet Elimox, tél. : +46-8-660-02-23, e-mail : '/>"/>

SOURCE OxThera
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