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Wilex AG Grillparzerstr. 10 81675 München, Germany http://www.wilex.com
Contact Ms Juliane Giese +49 89 41313829
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Wilex AG

WILEX erhält US FDA Genehmigung (IND) für klinische Phase II-Studie mit dem uPA-Inhibitor WX-671 bei Patienten mit Brustkrebs

(PresseBox) (München, )
Das Münchener biopharmazeutische Unternehmen WILEX AG (ISIN DE0006614720 / Frankfurter Wertpapierbörse / Prime Standard) gibt heute bekannt, dass es von der US-amerikanischen Zulassungsbehörde Food and Drug Administration (FDA) eine Investigational New Drug-Genehmigung (IND) zum Start einer Phase II-Studie mit dem Medikamentenkandidaten WX-671 erhalten hat. Die Studie untersucht die Wirksamkeit der Kombinationstherapie von WX-671 in Verbindung mit dem Chemotherapeutikum Capecitabine (Xeloda®, Hoffmann La Roche AG, Basel, Schweiz) bei Patienten mit metastasiertem, HER2-Rezeptor-negativem Brustkrebs. Damit wird die oral verabreichbare Substanz zur Hemmung des uPA-Systems jetzt in einer zweiten Phase II-Studie untersucht. Die Studie wird vom US-Verteidigungsministerium im Rahmen des Brustkrebsforschungsprogrammes unter der Vndxwmvsyeaacwzraxt AOKR43-79-9-4510 ejpvgaibiww.

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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.