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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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              title="Automatisch aus dem Englischen übersetzt. Standardsprache in den Einstellungen ändern.">EN</span>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/07/21/3330294/31990/en/Agios-Provides-Update-on-Phase-2-Trial-of-Tebapivat-in-Sickle-Cell-Disease.html">Agios informiert über Phase‑2‑Studie zu Tebapivat bei Sichelzellkrankheit</a>
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        Hämoglobin‑Ansprechraten für tebapivat, einen PK‑Aktivator, entsprachen der Medikamentenklasse, aber die Phase‑2‑Ergebnisse konnten kein differenziertes Profil nachweisen, das die Weiterentwicklung bei Sichelzellkrankheit stützt. Sicherheit und Verträglichkeit von tebapivat entsprachen früheren Studien bei Sichelzellkrankheit. sNDA für mitapivat, das grundlegende PK‑Aktivator‑Programm des Unter...
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      <a target="_blank" rel="nofollow" href="https://www.investors.com/news/technology/agios-stock-fda-priority-review-mitapivat-sickle-cell-disease-treatment/">Warum dieser Novo-Nordisk-Wettbewerber nahe einer Gewinnmitnahmezone stark anstieg</a>
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        Agios-Aktie schnellte am Dienstag in Richtung einer Gewinnmitnahmezone, nachdem die FDA seinem Sichelzellenmedikament eine beschleunigte Prüfung zugewiesen hatte.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/07/07/3323022/31990/en/U-S-FDA-Grants-Priority-Review-to-Agios-sNDA-for-Mitapivat-in-Sickle-Cell-Disease.html">US-FDA gewährt Agios Priority Review für sNDA zu Mitapivat bei Sichelzellenerkrankung</a>
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        Der PDUFA-Zieltermin der FDA ist der 1. November 2026 Wenn zugelassen, könnte Mitapivat das erste orale PK-Aktivator-Wirkstoff für Patienten mit Sichelzellenerkrankung werden CAMBRIDGE, Mass., 07. Juli 2026 (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), ein Unternehmen in kommerziellem Stadium, das sich auf die Bereitstellung innovativer Medikamente für Patienten mit seltenen E...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/13/3311392/31990/en/Agios-Showcases-RISE-UP-Phase-3-Results-at-EHA-2026-Plenary-Session-Reinforcing-Strong-Anti-Hemolytic-Profile-of-Mitapivat-in-Sickle-Cell-Disease.html">Agios Showcases RISE UP Phase 3 Results at EHA 2026 Plenary Session Reinforcing Strong Anti-Hemolytic Profile of Mitapivat in Sickle Cell Disease</a>
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        Mitapivat demonstrated statistically significant improvement in hemoglobin response compared with placebo, with rapid onset and durable effects New analyses showed patients in mitapivat arm had clinically meaningful reduction in transfusion burden compared with placebo Patients in mitapivat arm who achieved hemoglobin response had clinically meaningful benefits across measures of sickle cell pa...
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      <a target="_blank" rel="nofollow" href="https://www.proactiveinvestors.com/companies/news/1093235?SNAPI">Agios Pharmaceuticals licenses global rights to Oscotec&#39;s SYK inhibitor cevidoplenib</a>
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        Agios Pharmaceuticals (NASDAQ:AGIO) has secured exclusive global rights to cevidoplenib, a next-generation oral SYK inhibitor, under a licensing agreement with South Korea&#39;s Oscotec, the company said Monday. The agreement gives Agios worldwide rights to develop and commercialize cevidoplenib, which the company described as a novel, next-generation oral inhibitor of spleen tyrosine kinase (SYK).
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/01/3304100/31990/en/Agios-Enters-Exclusive-Global-License-Agreement-with-Oscotec-to-Develop-and-Commercialize-Next-Generation-SYK-Inhibitor-Cevidoplenib.html">Agios Enters Exclusive Global License Agreement with Oscotec to Develop and Commercialize Next-Generation SYK Inhibitor Cevidoplenib</a>
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        Agios obtains exclusive global rights to novel, late-stage, next-generation, oral SYK inhibitor Agreement diversifies Agios&#39; rare hematology portfolio with expansion into immune thrombocytopenia, unlocking up to $1 billion in peak U.S. sales potential Oscotec will receive $25.0 million upfront, with future payments tied to development, regulatory, and commercial milestones, as well as tiered ro...
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/agios-scraps-blood-cancer-drug-program-after-study-miss-2026-05-29/">Agios scraps blood cancer drug program after study miss</a>
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        Agios Pharmaceuticals said on Friday ​it will stop developing its ‌experimental drug for a form of blood cancer after a ​mid-stage trial failed to ​show enough benefit.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/29/3303496/31990/en/Agios-Provides-Update-on-Phase-2b-Trial-of-Tebapivat-in-Lower-Risk-Myelodysplastic-Syndromes.html">Agios Provides Update on Phase 2b Trial of Tebapivat in Lower-Risk Myelodysplastic Syndromes</a>
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        Results did not meet predefined threshold to support further development in LR-MDS Tebapivat was well tolerated, with no new safety signals observed CAMBRIDGE, Mass., May 29, 2026 (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company focused on delivering innovative medicines for patients with rare diseases, today announced that it will not...
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