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  <title>Zasocitinib (TAK-279) meets primary and secondary endpoints in Phase 3 plaque psoriasis studies</title>
  <pubDate>Thu, 22 Jan 2026 09:00:00 +0100</pubDate>
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  <title>Den första enzymersättningsterapin Adzynma (rekombinant ADAMTS13) för cTTP nu tillgänglig i Sverige</title>
  <pubDate>Tue, 24 Jun 2025 08:00:00 +0200</pubDate>
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  <title>ADHD i vardagen – en ny podd som vill göra tillvaron lite lättare </title>
  <pubDate>Fri, 11 Apr 2025 11:49:27 +0200</pubDate>
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  <title>Ny ADHD-app ska underlätta för personer som lever med ADHD</title>
  <pubDate>Fri, 14 Mar 2025 09:00:00 +0100</pubDate>
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  <title>Roland Kurney ny vd för Takeda Sverige</title>
  <pubDate>Tue, 04 Mar 2025 14:00:00 +0100</pubDate>
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  <title>Stor satsning på precisionsmedicin för inflammatorisk tarmsjukdom</title>
  <pubDate>Mon, 30 Sep 2024 12:30:50 +0200</pubDate>
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  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Stor kunskapssatsning inom sällsynta diagnoser: Ovanligt.se – unik och ambitiös plattform bidrar till personcentrerad vård</title>
  <pubDate>Thu, 29 Feb 2024 09:51:39 +0100</pubDate>
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  <title>Ovanligt.se – ny unik storsatsning ska synliggöra sällsynta diagnoser</title>
  <pubDate>Thu, 29 Feb 2024 09:43:03 +0100</pubDate>
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  <title>Takedas HYQVIA godkänd av Europeiska kommissionen som underhållsbehandling vid kronisk inflammatorisk demyeliniserande polyneuropati (CIDP) efter initiering med intravenösa immunoglobuliner</title>
  <pubDate>Fri, 02 Feb 2024 08:30:00 +0100</pubDate>
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  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Premiär för säsong två av Sällsynta Podden </title>
  <pubDate>Thu, 01 Feb 2024 08:00:00 +0100</pubDate>
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  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/premiaer-foer-saesong-tvaa-av-saellsynta-podden-3300657?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
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  <title>Ny svensk studie bekräftar ojämlikheter vid diagnos av adhd: Kvinnor får adhd-diagnos flera år senare än män – kan leda till ökad psykisk ohälsa</title>
  <pubDate>Mon, 04 Dec 2023 09:17:48 +0100</pubDate>
  <description>En svensk studie, Time after time, visar att kvinnor i genomsnitt diagnostiseras fyra år senare än män. Studien visar även på ökad samsjuklighet hos flickor och kvinnor där förekomsten av ångest och ätstörningar är starkt framträdande. Forskarna hoppas att studien belyser de komplexa utmaningar flickor och kvinnor med adhd möter och kan bidra till att minska ojämlikheter mellan kvinnor och män.</description>
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  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Denguefeber ökar i allt fler länder som är populära resmål för svenskar </title>
  <pubDate>Tue, 31 Oct 2023 11:31:03 +0100</pubDate>
  <description></description>
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  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/denguefeber-oekar-i-allt-fler-laender-som-aer-populaera-resmaal-foer-svenskar-3283115?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Takeda stärker digitalt initiativ och sätter fokus på flickor och kvinnor med ADHD</title>
  <pubDate>Tue, 28 Mar 2023 09:30:00 +0200</pubDate>
  <description></description>
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  <title>Nordic Rare Disease Summit samlar experter för att diskutera hur vården av patienter med sällsynta hälsotillstånd kan förbättras - i Stockholm den 17 april 2023</title>
  <pubDate>Thu, 09 Mar 2023 09:15:00 +0100</pubDate>
  <description></description>
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  <title>Sällsynta Podden – tredje avsnittet av den nya podcastserien om sällsynta sjukdomar ur ett patient- och anhörigperspektiv släpps idag</title>
  <pubDate>Tue, 31 Jan 2023 09:00:00 +0100</pubDate>
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  <title>Sällsynta Podden – andra avsnittet av den nya podcastserien om sällsynta sjukdomar ur ett patient- och anhörigperspektiv släpps idag</title>
  <pubDate>Mon, 16 Jan 2023 09:00:00 +0100</pubDate>
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  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Takedas Qdenga tetravalent, denguevaccin [levande, försvagat] godkänt för användning i EU.</title>
  <pubDate>Thu, 15 Dec 2022 14:33:34 +0100</pubDate>
  <description></description>
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  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/takedas-qdenga-tetravalent-denguevaccin-levande-foersvagat-godkaent-foer-anvaendning-i-eu-3224018?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Sällsynta Podden – ny podcastserie om sällsynta sjukdomar ur ett patient- och anhörigperspektiv</title>
  <pubDate>Wed, 14 Dec 2022 10:00:00 +0100</pubDate>
  <description></description>
  <guid>https://www.mynewsdesk.com/se/takeda/pressreleases/saellsynta-podden-ny-podcastserie-om-saellsynta-sjukdomar-ur-ett-patient-och-anhoerigperspektiv-3223429?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</guid>
  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/saellsynta-podden-ny-podcastserie-om-saellsynta-sjukdomar-ur-ett-patient-och-anhoerigperspektiv-3223429?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>EU-kommissionen godkänner Livtencity (maribavir) – ett nytt behandlingsalternativ för transplanterade patienter som drabbats av CMV-infektion som är svårbehandlad med eller utan resistens mot dagens standardbehandling</title>
  <pubDate>Tue, 29 Nov 2022 09:18:02 +0100</pubDate>
  <description></description>
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  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/eu-kommissionen-godkaenner-livtencity-maribavir-ett-nytt-behandlingsalternativ-foer-transplanterade-patienter-som-drabbats-av-cmv-infektion-som-aer-svaarbehandlad-med-eller-utan-resistens-mot-dagens-standardbehandling-3220436?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
  <dc:creator>Takeda Pharma AB</dc:creator>
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  <title>Takeda Receives Positive CHMP Opinion Recommending Approval of Dengue Vaccine Candidate in EU and Dengue-Endemic Countries</title>
  <pubDate>Thu, 20 Oct 2022 11:05:54 +0200</pubDate>
  <description>Positive Opinion for TAK-003 Based on 4.5 Years of Safety and Efficacy Data from Pivotal Phase 3 Trial of 20,000 Children and Adolescents Across Eight Dengue-Endemic Countries. Marketing Authorization Expected in Coming Months in Europe Followed by Regulatory Approvals in Latin America and Asia.</description>
  <guid>https://www.mynewsdesk.com/se/takeda/pressreleases/takeda-receives-positive-chmp-opinion-recommending-approval-of-dengue-vaccine-candidate-in-eu-and-dengue-endemic-countries-3212392?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</guid>
  <link>https://www.mynewsdesk.com/se/takeda/pressreleases/takeda-receives-positive-chmp-opinion-recommending-approval-of-dengue-vaccine-candidate-in-eu-and-dengue-endemic-countries-3212392?utm_source=rss&amp;utm_medium=rss&amp;utm_campaign=Subscription&amp;utm_content=current_news</link>
  <dc:creator>Takeda Pharma AB</dc:creator>
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