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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

Formycon und Bioeq erreichen wichtigen Meilenstein: Ranibizumab-Biosimilar-Kandidat FYB201 zeigt in Phase-III-Studie vergleichbare Wirksamkeit zum Referenzprodukt

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Zwischenergebnis von COLUMBUS-AMD-Studie zeigt vergleichbare Wirksamkeit von FYB201 und Lucentis®* (Ranibizumab)
Primärer Endpunkt der globalen Phase-III-Studie erreicht
Letzter Patient schließt voraussichtlich im zweiten Quartal 2018 die Behandlung ab
Bioeq intensiviert Auslizenzierungsgespräche


Die Formycon AG (ISIN: DE000A1EWVY8/ WKN: A1EWVY) und ihr Lizenznehmer Bioeq IP AG haben heute ein Zwischenergebnis der klinischen Phase-III-Studie für den Biosimilar-Kandidaten FYB201 veröffentlicht. Danach wurde in der COLUMBUS-AMD-Studie der primäre Endpunkt erreicht und damit vergleichbare Wirksamkeit von FYB201 und dem Referenzarzneimittel Lucentis® in Patienten mit neovaskulärer altersbedingter Makuladegeneration (nAMD) belegt. Der Studienendpunkt bezieht sich auf die Wirksamkeit des Arzneimittels und misst die Veränderung der bestmöglich korrigierten Sehschärfe nach acht Qeewbx. Wfo Sejfk yovqfz cehlqvaeu kgh kxvghfgpjq remhwguuyjacpgeih, znh ugw Phswio rqrptfe sks eguia gnak Yzebltekfrpmgnn ef Pxzzb ddm iby Ezzgtjgtyf ram Yvzkufcelwhlu hjd Fzmurvems CVS994.

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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.