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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Biogen-US09062X1037">Biogen</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/03/31/3265288/0/en/Biogen-to-Acquire-Apellis-Enhancing-the-Company-s-Growth-Portfolio-in-Immunology-and-Rare-Disease-Bolstering-Growth-Outlook-and-Accelerating-Expansion-into-Nephrology.html">Biogen to Acquire Apellis, Enhancing the Company&#39;s Growth Portfolio in Immunology and Rare Disease, Bolstering Growth Outlook and Accelerating Expansion into Nephrology</a>
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        CAMBRIDGE, Mass. and WALTHAM, Mass., March 31, 2026 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) and Apellis Pharmaceuticals, Inc. (Nasdaq: APLS) today announced the companies have entered into a definitive agreement under which Biogen has agreed to acquire all outstanding shares of Apellis for $41.00 per share in cash at closing, or approximately $5.6 billion. Apellis stockholders will also ...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Biogen-US09062X1037">Biogen</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.proactiveinvestors.com/companies/news/1089764?SNAPI">Biogen high-dose Spinraza approval seen supporting long-term growth</a>
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        The US Food and Drug Administration has approved a higher-dose version of Spinraza, a key therapy from Biogen Inc (NASDAQ:BIIB, XETRA:IDP) for spinal muscular atrophy (SMA), a move analysts at Jefferies say could help sustain the company&#39;s long-standing position in the rare disease market. According to the analysts, the decision was largely anticipated by investors despite earlier regulatory de...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Biogen-US09062X1037">Biogen</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-higher-dose-biogens-genetic-disorder-drug-2026-03-30/">US FDA approves higher-dose of Biogen&#39;s genetic disorder drug</a>
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        The U.S. ​Food and ‌Drug Administration has ​approved a ​higher-dose version of ⁠Biogen&#39;s ​drug for ​a rare genetic disorder ​that ​causes progressive muscle ‌weakness, ⁠offering patients a potentially more ​effective ​option, ⁠the company ​said ​on ⁠Monday.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/03/30/3264519/0/en/FDA-Approves-New-High-Dose-Regimen-of-SPINRAZA-nusinersen-for-Spinal-Muscular-Atrophy.html">FDA Approves New High Dose Regimen of SPINRAZA® (nusinersen) for Spinal Muscular Atrophy</a>
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        The approval was anchored on data from the pivotal DEVOTE study that investigated the efficacy and safety of the High Dose Regimen of SPINRAZA in treatment-naïve and previously treated SPINRAZA patients High Dose SPINRAZA will be available in the United States in the coming weeks and is also approved in the European Union, Switzerland and Japan CAMBRIDGE, Mass., March 30, 2026 (GLOBE NEWSWIRE) ...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/03/28/3264201/0/en/Biogen-Announces-Second-Positive-Phase-2-Litifilimab-Trial-in-Cutaneous-Lupus-Erythematosus-at-2026-American-Academy-of-Dermatology-Annual-Meeting-Showing-a-Significant-Reduction-i.html">Biogen Announces Second Positive Phase 2 Litifilimab Trial in Cutaneous Lupus Erythematosus at 2026 American Academy of Dermatology Annual Meeting, Showing a Significant Reduction in Skin Disease Activity</a>
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        CAMBRIDGE, Mass., March 28, 2026 (GLOBE NEWSWIRE) -- Biogen Inc. (Nasdaq: BIIB) announced positive results from the Phase 2 part of the AMETHYST Phase 2/3 study (Part A) of litifilimab in people living with cutaneous lupus erythematosus (CLE). Litifilimab is the first humanized IgG1 monoclonal antibody (mAb) targeting blood dendritic cell antigen 2 (BDCA2), which has the potential to become the...
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      <a target="_blank" rel="nofollow" href="https://www.prnewswire.com/news-releases/alteogen-enters-into-a-license-agreement-with-biogen-for-development-and-commercialization-of-hybrozyme-based-subcutaneous-biologics-302724668.html">Alteogen Enters into a License Agreement with Biogen for Development and Commercialization of Hybrozyme™-Based Subcutaneous Biologics</a>
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        - Biogen gains rights to develop and commercialize subcutaneous (SC) formulations for two products utilizing ALT-B4 DAEJEON, South Korea, March 25, 2026 /PRNewswire/ -- Alteogen Inc. (KOSDAQ: 196170) announced today that it has entered into an exclusive license agreement with Biogen Inc. for the development and commercialization of subcutaneous (SC) formulations of biologics utilizing ALT-B4 po...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Biogen-US09062X1037">Biogen</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.ad-hoc-news.de/boerse/news/ueberblick/biogen-inc-aktie-neue-real-world-daten-zu-leqembi-und-pipeline-update-am/68971869">Die Biogen Inc. Aktie (ISIN: US09062X1037) steht unter Druck, während neue Real-World-Daten zu Leqembi bei Alzheimer-Demenz und Fortschritte in der Tau-Pipeline Investoren aufhorchen lassen. Trotz monatlicher Verluste am Nasdaq in US-Dollar prüfen Analysten das Potenzial neuer Therapien genau.</a>
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        Biogen Inc. Aktie: Neue Real-World-Daten zu Leqembi und Pipeline-Update am Nasdaq sorgen für Bewegung
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/03/20/3259865/0/en/Results-from-Real-World-Long-Term-Treatment-Persistence-with-LEQEMBI-lecanemab-irmb-in-the-United-States-Presented-at-AD-PD-2026.html">Results from Real-World, Long-Term Treatment Persistence with LEQEMBI® (lecanemab-irmb) in the United States Presented at AD/PD™ 2026</a>
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        Real-World LEQEMBI Data Shows Patients Choose to Stay on Long-Term Treatment Real-World LEQEMBI Data Shows Patients Choose to Stay on Long-Term Treatment
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