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Formycon AG Fraunhoferstraße 15 82152 Martinsried/Planegg, Germany http://www.formycon.com
Contact Mr Thorsten Schüller +49 89 864667150
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Formycon AG

Biosimilar Candidate FYB201 Shows Efficacy Comparable to the Reference Product in Phase III Study

Interim top-line data of COLUMBUS-AMD trial show comparable efficacy of FYB201 to Lucentis®* (ranibizumab) / Primary endpoint of the phase III study achieved

(PresseBox) (Munich, )
Formycon AG (ISIN: DE000A1EWVY8/ WKN: A1EWVY) today announced that, according to an interim result, the primary endpoint has been achieved in the COLUMBUS-AMD phase III trial, which is intended to demonstrate the efficacy, safety and immunogenicity of FYB201 and the reference medicinal product Lucentis® in patients with neovascular age-related macular degeneration (nAMD). The primary endpoint relates to efficacy and measures the comparable change in best corrected visual acuity after eight weeks. The confidence interval lies within the pre-defined equivalence limits and demonstrates the comparable efficacy of FYB201 and Lucentis®.

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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.