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Jubilant Therapeutics Inc. présentera des données sur les inhibiteurs sélectifs de l'isoforme de PAD4 pour le traitement du cancer à la réunion annuelle 2022 de l'American Association of Cancer Research (AACR)
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Mar 11, 2022, 01:10 ET

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BEDMINSTER, N.J., 11 mars 2022 /PRNewswire/ -- Jubilant Therapeutics Inc. (« Jubilant »), une société biopharmaceutique qui développe des petites molécules thérapeutiques de précision pour répondre à des besoins médicaux non satisfaits en oncologie et dans le domaine des maladies auto-immunes, a annoncé aujourd'hui la présentation de données relatives aux inhibiteurs de la peptidylarginine désiminase type-4 (PAD4), une cible thérapeutique potentielle pour traiter le cancer et les maladies auto-immunes. La réunion aura lieu à l'American Association of Cancer Research Annual (AACR), à la Nouvelle-Orléans, du 8 au 13 avril 2022, en personne et virtuellement.

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Jubilant Therapeutics Inc. to Present Data on Isoform Selective PAD4 inhibitors in the Treatment of Cancer at the American Association of Cancer Research Annual (AACR) Meeting 2022
Jubilant Therapeutics Inc. to Present Data on Isoform Selective PAD4 inhibitors in the Treatment of Cancer at the American Association of Cancer Research Annual (AACR) Meeting 2022

Les détails de la présentation sont les suivants :

Objet : Nouveaux inhibiteurs sélectifs de l'isoforme de PAD4 pour le traitement du cancer 
Type de présentation : Affiche
Présentateurs : Luca Rastelli, directeur scientifique
Dhanalakshmi Sivanandhan, vice-présidente, Biologie de découverte
Séance : Nouvelles cibles et voies
Heure et date : 12 avril 2022, de 9 h à 12 h 30
Lien vers le résumé : https://www.abstractsonline.com/pp8/#!/10517/presentation/15071

À propos de la PAD4

La peptidylarginine désiminase type-4 (PAD4) est une enzyme qui transforme la protéine arginine, ou mono-méthyl arginine, en citrulline. La réaction d'hypercitrullination induite par la PAD4 sur les neutrophiles provoque le rejet de chromatine nucléaire pour former un réseau de chromatine appelé pièges extracellulaires des neutrophiles (NETs). Il a été démontré que les NETs sont associés à plusieurs processus pathologiques, y compris la métastase du cancer, la fibrose, l'accident vasculaire cérébral ischémique, la pré-éclampsie, la thrombose et d'autres maladies auto-immunes. Jubliant Therapeutics Inc. cible l'inhibition de la PAD4 comme nouvelle stratégie pour traiter la progression du cancer, la formation de métastases et les maladies auto-immunes sans induire d'immunosuppression comme c'est le cas avec la plupart des autres agents approuvés pour les maladies auto-immunes.

À propos de Jubilant Therapeutics, Inc.

Jubilant Therapeutics Inc. est une société biopharmaceutique axée sur le patient qui développe des modulateurs puissants et sélectifs à base de petites molécules pour répondre à des besoins médicaux non satisfaits en oncologie et dans le domaine des maladies auto-immunes. Son moteur de découverte avancé intègre la conception basée sur la structure et les algorithmes de calcul pour découvrir et développer de nouvelles thérapies de précision contre des cibles de premier ordre ou validées, mais difficiles à atteindre dans des populations de patients génétiquement définies. La société fait progresser son programme le plus avancé, le premier inhibiteur double de LSD1/HDAC6 de sa catégorie, jusqu'à la phase 1/2a au premier trimestre 2022, suivi par d'autres IND avec de nouveaux modulateurs de PRMT5 et PDL1 qui pénètrent dans le cerveau, ainsi que des inhibiteurs de PAD4 dans des indications oncologiques et inflammatoires. Le siège de Jubilant Therapeutics est situé à Bedminster NJ et est dirigé par des leaders d'opinion et des membres du conseil consultatif scientifique de renommée mondiale. Pour obtenir plus d'informations, veuillez consulter le site Web www.jubilanttx.com ou nous suivre sur Twitter @JubilantTx et sur LinkedIn.

Photo : https://mma.prnewswire.com/media/1764087/Jubliant_AACR_Meeting_2022.jpg
Logo : https://mma.prnewswire.com/media/1064788/Jubilant_Therapeutics_Logo.jpg

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