Entity
  • Foundation For Rare Diseases

    Created in 2012
  • Social networks

    3,123 5,839
  • Activities

  • Entity types

  • Location

    96 Rue Didot, 75014 Paris, France

    Paris

    France

  • Employees

    Scale: 11-50

    Estimated: 20

  • SIREN

    751931445
  • Engaged corporates

    20
    5 13
  • Added in Motherbase

    5 years ago
Description
  • Value proposition

    Foundation for Scientific Cooperation

    The French Foundation for rare diseases (Fondation maladies rares) is a unique cooperative framework dedicated to rare diseases research. Co-founded by French University Hospitals, Universities, Research organisations and Patients’ organizations, it acts as a strategic hub to coordinate, federate and fund rare diseases research, essentially at the French national level.
    The French Foundation for rare diseases is a non-profit private structure, created in February 2012.
    Its support spans from basic, translational and clinical sciences to social and human research towards effective health care for patients affected by rare diseases. The Foundation has built strong links with its co-founders as well as several partnerships with private companies and is welcoming the development of additional partnerships to make the rare diseases issue better integrated in companies'​ health policies.
    The Foundation brings financial support to innovative projects and stimulates cross-sector cooperation to accelerate scientific, medical and social innovations to the patients’ benefit. Priorities are driven by grounded needs.

    Chercheur, Fondation, Accompagnement, maladie rare, santé, recherche santé, rare, projet scientifique, and fondation maladies rares

  • Original language

    Fondation de coopération scientifique

    La Fondation Maladies Rares est un acteur engagé dans la recherche de nouveaux traitements.

    La Fondation Maladies Rares a deux missions :
    ► décrypter les maladies rares en aidant au diagnostic et au développement de nouveaux médicaments
    ► améliorer le quotidien des personnes concernées

    Pour cela, elle finance et accompagne des projets de recherche ciblés, répondant à un besoin précis sans réponse à ce jour. Ses interventions concernent donc des maillons manquants indispensables à l'avancée des projets.
    Elle réunit les meilleures expertises et donne les moyens aux différents acteurs de travailler ensemble pour accélérer le développement de nouveaux traitements.

    La Fondation Maladies Rares existe depuis 5 ans et les résultats sont déjà spectaculaires avec plus de 267 projets de recherche soutenus.
    Son défi continue car il y a aujourd’hui plus de 7 000 maladies rares qui touchent 3 millions de personnes en France dont près de la moitié sont des enfants ... et 97% de ces maladies n’ont pas de traitement.

    Découvrez ce qu'est la Fondation ? https://youtu.be/dpLb74OVprc

    More informations on the Foundation For Rare Diseases : https://fondation-maladiesrares.org/eng/

  • Fondation Maladies Rares - Trouvons des traitements

    La Fondation Maladies Rares favorise la conduite de projets de recherche scientifique ainsi que le partage de connaissances sur les maladies rares.

  • https://fondation-maladiesrares.org/
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