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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">Investors Business Daily</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.investors.com/news/technology/takeda-pharmaceutical-ai-designed-psoriasis-pill-bristol-myers-squibb-sotyktu/">Takeda Designed A Psoriasis Pill Using AI. It Just Walloped Bristol&#39;s Sotyktu In A Head-To-Head Test.</a>
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        Takeda said Thursday its AI-designed psoriasis pill, zasocitinib, easily beat Bristol&#39;s Sotyktu in a head-to-head study.
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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">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/takedas-ai-crafted-psoriasis-pill-tops-bristol-myers-sotyktu-head-to-head-trial-2026-06-11/">Takeda&#39;s AI-crafted psoriasis pill tops Bristol Myers&#39; Sotyktu in head-to-head trial</a>
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        Japan&#39;s Takeda Pharmaceutical said on Thursday its experimental once-daily psoriasis pill, developed with the help of AI, outperformed Bristol Myers Squibb&#39;s approved ​drug Sotyktu in a late-stage head-to-head study.
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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">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260611341613/en/Takeda%E2%80%99s-Zasocitinib-Significantly-Outperforms-Deucravacitinib-in-Head-to-Head-Phase-3-Psoriasis-Study-Promising-to-Redefine-Oral-Treatment-Expectations/">Takeda&#39;s Zasocitinib Significantly Outperforms Deucravacitinib in Head-to-Head Phase 3 Psoriasis Study, Promising to Redefine Oral Treatment Expectations</a>
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        OSAKA, Japan &amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) announced positive topline results for the Phase 3, randomized, multicenter, double-blind study comparing zasocitinib (TAK-279), an investigational, next-generation, highly selective and potent oral tyrosine kinase 2 (TYK2) inhibitor, to deucravacitinib in adults with moderate-to-severe plaque psoriasis (PsO). In the L...
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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">4 months ago</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260608352333/en/U.S.-FDA-Accepts-Takedas-Application-for-Intravenous-ENTYVIO%C2%AE-vedolizumab-in-Pediatric-Ulcerative-Colitis-and-Crohns-Disease/">U.S. FDA Accepts Takeda&#39;s Application for Intravenous ENTYVIO® (vedolizumab) in Pediatric Ulcerative Colitis and Crohn&#39;s Disease</a>
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        OSAKA, Japan &amp; CAMBRIDGE, Mass.--(BUSINESS WIRE)--Takeda (TSE:4502/NYSE:TAK) today announced the U.S. Food and Drug Administration (FDA) has accepted for review its supplemental Biologics License Application (sBLA) for intravenous (IV) ENTYVIO® (vedolizumab) for the treatment of moderately to severely active ulcerative colitis (UC) and Crohn&#39;s disease in pediatric patients ages 2 years and olde...
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