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          Positive
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Proactive Investors</div>
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        <div class="me-2 text-gray">4 months ago</div>
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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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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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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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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">4 months ago</div>
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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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          Neutral
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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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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          Neutral
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260522186975/en/Avanzanite-Bioscience%E2%80%99s-Partner-Agios-Announces-PYRUKYND%C2%AE-mitapivat-Approval-in-the-European-Union-for-Adults-with-Thalassaemia/">Avanzanite Bioscience&#39;s Partner Agios Announces PYRUKYND® (mitapivat) Approval in the European Union for Adults with Thalassaemia</a>
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        AMSTERDAM--(BUSINESS WIRE)-- #Avanzanite--Avanzanite Bioscience B.V., a rapidly growing commercial-stage European specialty pharmaceutical company focused on rare diseases, today reported that its partner, Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company headquartered in Cambridge, Massachusetts focused on delivering innovative medicines for patients with...
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          Neutral
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/22/3300143/31990/en/Agios-PYRUKYND-mitapivat-Approved-in-the-European-Union-for-Adults-with-Thalassemia.html">Agios&#39; PYRUKYND® (mitapivat) Approved in the European Union for Adults with Thalassemia</a>
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        PYRUKYND is the only medicine approved in the EU for adults with transfusion-dependent and non-transfusion-dependent alpha- or beta-thalassemia Mitapivat is now approved for thalassemia in the U.S., Saudi Arabia, United Arab Emirates, and EU Avanzanite Bioscience B.V., a specialty pharmaceutical company, will continue to distribute and commercialize PYRUKYND in Europe CAMBRIDGE, Mass.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/12/3293011/31990/en/Agios-Submits-sNDA-to-FDA-for-U-S-Accelerated-Approval-of-Mitapivat-in-Sickle-Cell-Disease.html">Agios Submits sNDA to FDA for U.S. Accelerated Approval of Mitapivat in Sickle Cell Disease</a>
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        sNDA submission follows agreement with FDA on confirmatory trial, a requirement of the accelerated approval pathway Confirmatory trial designed to demonstrate clinical benefit of mitapivat on reducing transfusion burden in sickle cell disease CAMBRIDGE, Mass., May 12, 2026 (GLOBE NEWSWIRE) -- Agios Pharmaceuticals, Inc. (Nasdaq: AGIO), a commercial-stage biopharmaceutical company focused on del...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Agios-Pharmaceuticals-Inc-US00847X1046">Agios Pharmaceuticals, Inc.</a></div>
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        <div class="me-2 text-gray">5 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/12/3292999/31990/en/Agios-to-Present-New-Data-at-EHA-2026-Reinforcing-the-Significant-Therapeutic-Impact-of-Mitapivat-Across-Multiple-Rare-Hemolytic-Anemias.html">Agios to Present New Data at EHA 2026 Reinforcing the Significant Therapeutic Impact of Mitapivat Across Multiple Rare Hemolytic Anemias</a>
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        Detailed results from RISE UP Phase 3 trial of mitapivat in sickle cell disease selected for distinguished Plenary Abstracts Session Company to host investor conference call and webcast during EHA 2026 on Saturday, June 13, at 9:00 a.m. ET (3:00 p.m.
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