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SYGNIS gibt Abschluss der Patientenuntersuchung zur AXIS 2-Studie bekannt

(PresseBox) (Heidelberg, )
Die SYGNIS Pharma AG (Frankfurt: LIOK; ISIN DE000A1E9B74; Prime Standard), die sich auf die Erforschung und Entwicklung neuer Therapien zur Behandlung von Erkrankungen des Zentralen Nervensystems spezialisiert hat, gab heute den Abschluss der Patientenuntersuchung zu ihrer plazebo-kontrollierten, doppelverblindeten klinischen Phase 2-Wirksamkeitsstudie für AX200 zur Behandlung des akuten Schlaganfalls (AXIS 2) bekannt, in welcher 328 Patienten in acht europäischen Ländern behandelt wurden.

Mit dem multiplen Therapieansatz, welcher insbesondere den Zelltod in der akuten Phase des Schlaganfalls stoppt sowie die Regeneration des bereits geschädigten Gehirns fördert, bietet AX200 einen völlig neuartigen Therapieansatz zur Behandlung von Schlaganfallpatienten.

Dr. Frank Rathgeb, Forschungs-
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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.