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

Posted on by par Posté dans Communication Officielle, Medicine Théragenomique, Thasso Poste, Thérapie Génique Aucun commentaire ↓

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

Posted on by par Posté dans La Presse, Medicine Théragenomique, Prédisposition génétique, Thasso Poste, Thérapie Génique Aucun commentaire ↓

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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RSS random genetics

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    Many people in the U.S. do not belong to Native American communities but still carry bits of Native American DNA, inherited from European and African ancestors who had children with indigenous individuals during colonization and settlement. In a new study published 19th September in PLOS Genetics, Andrew Conley of the Georgia Institute of Technology and […]
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    A method to create a faster and lower cost alternative for a gene therapy tool has been developed by Boston University School of Medicine (BUSM) researchers.
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    A German and British research team lead by Technical University of Munich (TUM) has examined the interplay between genetics, cardiovascular disease and educational attainment in a major population study. Genetic variants which had been linked to educational attainment in other studies were observed in the subjects. The researchers found that these variants also had implications […]
  • Scientists develop new methodology to genetically modify lab mice and human cells septembre 19, 2019
    A team led by Cedars-Sinai has designed a rapid method to genetically alter laboratory mice and then used this method to produce personalized animal models of pediatric glioma, an aggressive type of malignant brain cancer in children.
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