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L'autorité américaine FDA a fixé une date cible PDUFA pour la demande d'enregistrement de PA21

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A la suite de la nouvelle demande d'enregistrement (NDA) de PA21, la Food and Drug Administration (FDA) américaine a annoncé qu'elle avait accepté le dossier et indiqué la date cible PDUFA (Prescription Drug User Fee Act) du 1er décembre 2013.

PA21, sous forme de comprimé à mâcher, est un adsorbant de phosphate à base de fer pour le traitement de l'hyperphosphatémie chez les patients atteints d'insuffisance rénale chronique (IRC). L'étude clinique pivot de phase III a montré que le nouvel adsorbant de phosphate permet de contrôler l'hyperphosphatémie chez les patients souffrant d'IRC tout en présentant l'avantage d'une posologie réduite.

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The publisher indicated in each case (see company info by clicking on image/title or company info in the right-hand column) is solely responsible for the stories above, the event or job offer shown and for the image and audio material displayed. As a rule, the publisher is also the author of the texts and the attached image, audio and information material. The use of information published here is generally free of charge for personal information and editorial processing. Please clarify any copyright issues with the stated publisher before further use. In case of publication, please send a specimen copy to service@pressebox.de.