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ANSM et le thérapie génique: accès précoce aux premiers médicaments innovants “CAR T-Cells”

27 juillet 2018 –  Cette point d’information vient de l’Agence nationale de sécurité du médicament et des produits de santé (ANSM) concernant l’accès précoce aux premiers médicaments innovants “CAR T-Cells” dans le traitement de certains cancers hématologiques.

En juin 2018, l’Agence européenne des médicaments (EMA) a rendu un avis positif pour l’autorisation de mise sur le marché des deux premiers médicaments de thérapie génique Kymriah et Yescarta appelés “CAR T-Cells”,

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Luxturna contre la cécité vendu 850 000 dollars

o4 janvier 2018 – Aux États-Unis, le médicament contre une dégénérescence rétinienne rare et héréditaire pouvant évoluer vers la cécité totale, le Luxturna sera vendu 850.000 dollars (425.000 dollars par oeil). Le prix final reste en dessous d’un million de dollars initialement évoqué mi-décembre lorsque son fabricant,

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  • New candidate cancer genes identified using math models novembre 15, 2019
    Computational modeling is the use of computers to simulate and study the behavior of complex systems. Computational approaches are widely adopted in the bioimedical sciences and can be used to sift through large volumes of complex data to extract recurrent patterns that may point to a disease's causes and effects.
  • Turning 'junk' DNA into gold novembre 15, 2019
    Mining the rich uncharted territory of the genome or genetic material of a cancer cell has yielded gold for Princess Margaret scientists: new protein targets for drug development against prostate cancer.
  • Researchers take first step toward genetic test for childhood short-sightedness novembre 15, 2019
    Researchers from the Universities of Cardiff and Bristol have devised a test that could in future help to identify children at risk of developing a very common eye condition.
  • Researchers link sisters' paralysis to an 'extremely rare' genetic variant novembre 15, 2019
    Following a nearly 25-year search across three continents, parents of a pair of sisters—who as children slowly became paralyzed from the waist down—finally have a diagnosis, according to researchers at University of Southern California (USC) and Translational Genomics Research Institute (TGen), an affiliate of City of Hope.
  • Genetic variation in individual brain cell types may predict disease risk novembre 15, 2019
    One might think that the primary cause of most genetically linked diseases comes from mutations in coding DNA—alterations in coding regions of the genome that can lead directly to changes in the expression of particular proteins important for a healthy body. But the majority of human DNA is non-coding DNA—regions of DNA that do not […]
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