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DE000A1EWVY8
Mon, 03.03.2025       Formycon AG

Press Release // March 3, 2025   FYB202/Otulfi ® (ustekinumab-aauz), a biosimilar to Stelara®, launched in the United States and the European Union FYB202/Otulfi ® is now commercially available in both subcutaneous and intravenous formulations in the United States and the European Union Patient transition to Otulfi® supported by comparable effic [ … ]
Tue, 25.02.2025       Formycon AG

Press Release // February 25, 2025   Formycon receives regulatory approval in the UK for FYB203 (aflibercept), a biosimilar to Eylea®, under the brand name AHZANTIVE® FYB203 (aflibercept) approved in the UK for the treatment of neovascular age-related macular degeneration (nAMD) and several other severe retinal diseases UK market authorization [ … ]
Mon, 24.02.2025       Formycon AG

Company Name: Formycon AG ISIN: DE000A1EWVY8   Reason for the research: Update Recommendation: Buy from: 24.02.2025 Target price: €46 Target price on sight of: 12 months Last rating change: - Analyst: Simon Scholes First Berlin Equity Research has published a research update on Formycon AG (ISIN: DE000A1EWVY8). Analyst Simo [ … ]
Thu, 20.02.2025       Formycon AG

 Press Release // February 20, 2025   Formycon presents clinical data on ustekinumab biosimilar FYB202 at the ECCO Congress in Berlin   Planegg-Martinsried, Germany - Formycon AG (FSE: FYB, Prime Standard, “Formycon”) will present an overview of the comparative data of the ustekinumab biosimilar FYB202 at this year's Congress of the European Croh [ … ]
Mon, 17.02.2025       Formycon AG

Press Release // February 17, 2025 Formycon AG informs about recent developments in various biosimilar projects and invites to conference call   Formycon continues FYB206 development without Phase III trial and thus takes pioneering role among pembrolizumab biosimilar developers; investment savings expected to amount to a high double-digit millio [ … ]
Mon, 17.02.2025       Formycon AG

Disclosure of inside information according to Article 17 of the Regulation (EU) No 596/2014 Formycon announces decision on Phase III trial with FYB206 and provides update on potential need to adjust the valuation of FYB202 and FYB201 Formycon terminates Phase III study ("Lotus") for FYB206 following positive feedback from the U.S. Food and Drug A [ … ]
Wed, 05.02.2025       Formycon AG

Press Release // February 05, 2025   Lotus Pharmaceutical becomes strategic partner for the commercialization of Formycon’s Eylea® biosimilar FYB203/AHZANTIVE® in the Asia-Pacific Region   Planegg-Martinsried, Germany – Klinge Biopharma GmbH (“Klinge”), the exclusive owner of the global commercialization rights of FYB203/AHZANTIVE®1 (aflibercept [ … ]
Mon, 20.01.2025       Formycon AG

Press Release // January 20, 2025 Formycon receives EU approval for FYB203 (aflibercept), a biosimilar to Eylea®, under the brand names AHZANTIVE® and Baiama® FYB203 (aflibercept) approved for the treatment of neovascular age-related macular degeneration (nAMD) and several other severe retinal diseases AHZANTIVE® and Baiama® offer patients treat [ … ]
Wed, 15.01.2025       Formycon AG

Press Release // January 15, 2025 Formycon and Fresenius Kabi announce MHRA approval for FYB202/Otulfi® (ustekinumab), a biosimilar to Stelara® Otulfi®received MHRA approval for both subcutaneous and intravenous formulations, to treat serious inflammatory diseases UK approval follows the series of successful approvals by the FDA, the European Co [ … ]
Mon, 13.01.2025       Formycon AG

Presse Release // January 13, 2025   Teva becomes strategic commercialization partner for Formycon’s biosimilar candidate FYB203 (Eylea®/ aflibercept) in major parts of Europe and Israel Planegg-Martinsried, Germany – Klinge Biopharma GmbH (Klinge), the licensee and exclusive global commercialization rights holder for FYB203, Formycon’s biosimila [ … ]

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Wednesday, 12.03.2025, Calendar Week 11, 71st day of the year, 294 days remaining until EoY.