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      Pharnext présente PXT-3003 au congrès biennal 2015 de la Société du Nerf Périphérique


      News provided by

      Pharnext SAS

      Jun 30, 2015, 02:00 ET

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      PARIS, le 30 Juin 2015 /PRNewswire/ -- Pharnext SAS annonce que les données de PXT-3003, actuellement en développement pour le traitement de la maladie de Charcot-Marie-Tooth de Type 1A (CMT1A), seront présentées sur quatre posters et lors d'une présentation orale au congrès biennal 2015 de la Société du Nerf Périphérique (PNS) au Centre des Congrès de Québec, Canada du 27 juin au 2 juillet 2015.

      Lors de la 4e session de posters, quatre posters seront présentés mercredi 1er juillet de 17h à 19h :

      Poster 23: "A Meta-Analysis Of Randomized Double-Blind Clinical Trials in CMT1A to Assess the Change from Baseline In CMTNS and ONLS Scales After One Year Of Treatment." Mandel J, et al. Vous pouvez accéder à la publication dans l'Orphanet Journal of Rare Diseases en cliquant sur le lien suivant: http://www.ojrd.com/content/10/1/74/abstract.

      Poster 35: "Design of the Next Phase III Trial Aiming to Confirm Efficacy and Safety of PXT-3003 in the Treatment of Charcot-Marie-Tooth Disease Type 1A." Scart-Grès C, et al.

      Poster 57: "An Online Survey of Neurologists about Charcot-Marie-Tooth Disease Type 1A." Paoli X, et al.

      Poster 62: "Baseline Analysis of PXT-3003 Phase 2 Data Reveals Two Blood Early Candidate Biomarkers for Therapeutic Response in CMT1A." Laffaire J, et al.

      Lors de la conférence plénière et de la 3e session sur les plateformes, le lundi 29 Juin de 9h55 à 10h10 :

      Présentation orale (Poster 310): "An Experimental Trial of an Early Onset Treatment with a Combinational Drug (PXT-3003) Consisting of Baclofen, Naltrexone, Sorbitol in the CMT1A Rat Model." Prukop T, et al ; Présenté par l'Institut Max Planck dans le cadre d'une collaboration avec Pharnext.

      A propos de Pharnext

      Pharnext est une société biopharmaceutique qui développe de nouveaux traitements ciblant simultanément plusieurs mécanismes  pathologiques dans des maladies neurologiques sévères, rares ou communes. La plateforme propriétaire de R&D de Pharnext s'appuie sur la pharmacologie des réseaux biologiques et est applicable à un large spectre de maladies. Elle permet le développement rapide de combinaisons synergiques de médicaments déjà utilisés dans d'autres maladies et dont le profil de sécurité est déjà établi: les pléomédicaments. Les deux principaux pléomédicaments de Pharnext sont PXT-3003 pour le traitement de la maladie orpheline Charcot-Marie-Tooth de type 1A (Phase 2 terminée) et PXT-864 pour la maladie d'Alzheimer (Phase 2 en cours) et d'autres pathologies neurologiques (notamment la maladie de Parkinson et la sclérose latérale amyotrophique).

      Pour plus d'informations, connectez-vous sur www.pharnext.com.

      Contact Pharnext
      Catherine Scart-Gres, M.D.
      Directrice des Affaires Médicales
      [email protected]  

      Contacts Média
      Caroline Carmagnol
      Valentine Boivin
      Alize RP
      Tél : 01 44 54 36 63
      [email protected]

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