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          Negative
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">28 days ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/trump-administration-announce-drug-pricing-deals-2026-08-31/">Trump administration to announce drug pricing deals</a>
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        U.S. President Donald ​Trump is expected to announce a new round of drug-pricing agreements on Monday, a White ‌House official said, part of a push to make healthcare more affordable for Americans.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
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        <div class="me-2 text-gray">Business Wire</div>
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        <div class="me-2 text-gray">about one month ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260824773270/en/Takeda-Receives-U.S.-FDA-Approval-of-MIMRYLO%E2%84%A2-rusfertide-Marking-a-Potential-Shift-in-the-Treatment-Paradigm-for-Polycythemia-Vera/">Takeda Receives U.S. FDA Approval of MIMRYLO™ (rusfertide), Marking a Potential Shift in the Treatment Paradigm for Polycythemia Vera</a>
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        OSAKA, Japan &amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) announced U.S. Food and Drug Administration (FDA) approval of the New Drug Application (NDA)* for MIMRYLO™ (rusfertide) for the treatment of erythrocytosis in adults with polycythemia vera (PV), a blood cancer. MIMRYLO is a first-in-class hepcidin mimetic designed to regulate iron distribution in the body and red blood...
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          Positive
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
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        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">about one month ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/legal/litigation/us-fda-approves-takeda-protagonists-drug-rare-blood-cancer-2026-08-28/">US FDA approves Takeda, Protagonist&#39;s drug for rare blood cancer</a>
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        The U.S. ​Food and ‌Drug Administration ​has approved a ​first-of-its-kind drug from ⁠Takeda ​Pharmaceutical and ​Protagonist Therapeutics to treat ​a ​rare blood cancer, the ‌health ⁠regulator said on ​Friday.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
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        <div class="me-2 text-gray">Business Wire</div>
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        <div class="me-2 text-gray">about one month ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260818063761/en/ORZEYFUL-oveporexton-Approved-in-Japan-as-the-First-and-Only-Medicine-to-Treat-the-Underlying-Cause-of-Narcolepsy-Type-1/">ORZEYFUL (oveporexton) Approved in Japan as the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1</a>
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        OSAKA, Japan &amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TOKYO:4502/NYSE:TAK) announced that the Japanese Ministry of Health, Labour and Welfare (MHLW) approved the use of ORZEYFUL (oveporexton) for the treatment of narcolepsy type 1 (NT1, narcolepsy with cataplexy) in adults. ORZEYFUL is a first-in-class oral orexin receptor 2 (OX2R) agonist and the only medicine indicated in Japan to treat t...
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          Neutral
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Business Wire</div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260805760759/en/U.S.-FDA-Approves-Takeda%E2%80%99s-ORZEYFUL%E2%84%A2-oveporexton-the-First-and-Only-Medicine-to-Treat-the-Underlying-Cause-of-Narcolepsy-Type-1/">U.S. FDA Approves Takeda&#39;s ORZEYFUL™ (oveporexton), the First and Only Medicine to Treat the Underlying Cause of Narcolepsy Type 1</a>
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        OSAKA, Japan &amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) announced that the U.S. Food and Drug Administration (FDA) approved ORZEYFUL™ (oveporexton), an oral orexin receptor 2 (OX2R) agonist, for the treatment of narcolepsy type 1 (NT1, narcolepsy with cataplexy) in adults.* The persistent 24-hour nature of NT1 is driven by orexin deficiency and can severely impact people&#39;s ...
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          Positive
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Reuters</div>
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        <div class="me-2 text-gray">about 2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/us-fda-approves-takedas-sleep-disorder-pill-2026-08-05/">US FDA approves Takeda&#39;s sleep disorder pill</a>
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        The FDA has approved Takeda Pharmaceuticals&#39; oral drug for narcolepsy, the U.S. ​health regulator said on Wednesday, backing ‌the first treatment that targets all the symptoms of the rare sleep disorder.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
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          <img class="news-box__source-logo" alt="StocksGuide" src="https://stocksguide.com/assets/logos/stocks_guide-94bb1add.svg" />
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        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">2 months ago</div>
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      <a data-turbo-frame="_top" href="https://stocksguide.com/en/stock/Takeda-Pharmaceutical-JP3463000004#earnings-events-section">Takeda Pharmaceutical Q1 2027 Earnings Call Transcript and Presentation available</a>
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        Show summary
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          <span class="news-box__logo-label">Earnings Call Transcript</span>
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/en/stock/Takeda-Pharmaceutical-JP3463000004">Takeda Pharmaceutical</a></div>
        <div class="me-2 text-gray text-size-10">●</div>
        <div class="me-2 text-gray">Business Wire</div>
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        <div class="me-2 text-gray">2 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260727883646/en/Takeda-Announces-FY2026-First-Quarter-Results-Near-Term-Launch-Preparations-and-Pipeline-Progress-on-Track/">Takeda Announces FY2026 First Quarter Results, Near-Term Launch Preparations and Pipeline Progress on Track</a>
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        OSAKA, Japan--(BUSINESS WIRE)--Takeda (TOKYO:4502/NYSE:TAK) announced financial results for the first quarter of fiscal year 2026 (April 1, 2026 to June 30, 2026), marking a period of disciplined execution and operational momentum. Takeda leveraged the resilient performance of its core in-line portfolio to support its long-term strategy, advancing commercial launch preparations and driving crit...
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