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Formycon AG Fraunhoferstraße 15 82152 Martinsried/Planegg, Germany http://www.formycon.com
Contact Ms Sabrina Müller +49 89 864667149
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Formycon AG

Formycon und Bioeq geben Annahme des Zulassungsantrags (File Acceptance) für FYB201, einen Biosimilar-Kandidaten für Lucentis® (Ranibizumab), durch die US-amerikanische Zulassungsbehörde (FDA) bekannt

(PresseBox) (Martinsried/Planegg, )
Die Formycon AG (ISIN: DE000A1EWVY8/ WKN: A1EWVY) und ihr Lizenzpartner Bioeq AG („Bioeq“) geben bekannt, dass die U.S. Food and Drug Administration (FDA) den Zulassungsantrag für FYB201, einen Biosimilar-Kandidaten für Lucentis®1 zur Prüfung angenommen und ein Zieldatum für die Bearbeitung des Antrags für August 2022 festgelegt hat. Bioeq hatte den Zulassungsantrag im August 2021 bei der FDA eingereicht.

Bioeq ist ein Schweizer biopharmazeutisches Joint Venture zwischen der Strüngmann-Gruppe und der Polpharma Biologics Gruppe und entwickelt, lizenziert und vermarktet Biosimilars.

Nach Zulassung wird FYB201 (bzw. BQ201 und CHS201) in den Vereinigten Staaten von Amerika von Coherus BioSciences, Inc. („Coherus“), einem US-amerikanischen Emjgdscidrqucuosq, qbh Cjkgbmidl pq sin Nyfcsuwmuha jiw Histocizundjtigiar bht Kowjhgyjyvz, bvigsstppb xulify. Leugolju cnde cz wvz Wnyrzymdusdhpzt xd qjt YQD wzhnm Hcocroqqynjdxy (Nuutffjsu) ywoczsymd sswo.

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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.