NEURONAX obtient l’autorisation de démarrer son étude clinique de
phase I en France et en Belgique e
NEURONAX, la société biopharmaceutique spécialisée dans la régénération neuronale, annonce avoir reçu l’autorisation de débuter son essai clinique de phase I de la part des autorités de santé (Agence Nationale pour la Sécurité des Médicaments (ANSM) pour la France et Agence Fédérale des Médicaments et des Produits de Santé (AFMPS) pour la Belgique). Ce premier essai clinique chez l’Homme avec le produit NX210 est intitulé «Etude de
phase I évaluant la sécurité et l’activité
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