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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Ionis-Pharmaceuticals-Inc-US4622221004">Ionis Pharmaceuticals, Inc.</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.barrons.com/articles/astrazeneca-stock-ionis-trial-failure-alnylam-40eab20f">AstraZeneca-Aktie und Partner Ionis stürzen nach Studienmisserfolg ab. Alnylam schießt nach oben.</a>
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      <div class="me-0 me-md-5">
        AstraZeneca und das kalifornische Biotechunternehmen Ionis Pharmaceuticals melden ein Scheitern der zulassungsrelevanten Studie für ihr Gen-Silencing-Medikament Wainua.
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        <div class="me-2 text-gray">vor 4 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.reuters.com/business/healthcare-pharmaceuticals/astrazeneca-ionis-drug-fails-meet-main-goal-late-stage-heart-disease-trial-2026-07-09/">AstraZeneca-Ionis-Medikament verfehlt primären Endpunkt in zulassungsrelevanter Herzstudie</a>
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        AstraZeneca teilte am Donnerstag mit, dass sein gemeinsam mit Ionis entwickeltes Medikament Wainua in einer zulassungsrelevanten Spätphase-Studie das Hauptziel, die Reduktion von kardiovaskulären Todesfällen und wiederkehrenden Herzproblemen, nicht erreicht habe.
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        <div class="me-2 text-gray">vor 4 Monaten</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.businesswire.com/news/home/20260708332180/en/Update-on-CARDIO-TTRansform-Phase-3-trial-of-eplontersen-in-adults-with-transthyretin-mediated-amyloid-cardiomyopathy/">Update zur zulassungsrelevanten Phase‑3‑Studie CARDIO‑TTRansform von Eplontersen bei Erwachsenen mit transthyretinvermittelter Amyloidkardiomyopathie</a>
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      <div class="me-0 me-md-5">
        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) und Partner AstraZeneca teilten heute mit, dass die zulassungsrelevante Phase‑3‑Studie CARDIO‑TTRansform für Eplontersen bei Patienten mit transthyretinvermittelter Amyloidkardiomyopathie (ATTR‑CM) den primären Wirksamkeitsendpunkt – das zusammengesetzte Ergebnis aus kardiovaskulärer (CV) Mortalität und wiederkehrende...
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        <div class="me-2 text-gray">vor 4 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260706516467/en/Ionis-completes-enrollment-in-pivotal-cohort-of-the-Phase-3-REVEAL-study-evaluating-obudanersen-in-Angelman-syndrome/">Ionis schließt Einschreibung in zulassungsrelevanten Kohortenabschnitt der Phase‑3‑Studie REVEAL zur Bewertung von obudanersen bei Angelman‑Syndrom ab</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) gab heute bekannt, dass die Einschreibung in der zulassungsrelevanten Kohorte (Kohorte 1) der globalen Phase‑3‑Studie REVEAL zur Bewertung von obudanersen (ION582), einem experimentellen RNA‑gerichteten Arzneimittel für Menschen mit Angelman‑Syndrom (AS), einer schweren und seltenen neurodevelopmentalen Störung, die m...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260624743930/en/Ionis-announces-license-agreement-with-Recordati-for-zilganersen-in-Alexander-disease-AxD-in-all-countries-outside-the-U.S./">Ionis announces license agreement with Recordati for zilganersen in Alexander disease (AxD) in all countries outside the U.S.</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced that it has entered into a license agreement with Recordati (“Recordati”), under which Recordati obtained exclusive rights to develop and commercialize zilganersen, an investigational RNA-targeted medicine for Alexander disease (AxD), in all countries outside the U.S. Ionis will maintain sole commercia...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260624119051/en/TRYNGOLZA%C2%AE-olezarsen-approved-by-the-FDA-as-the-first-and-only-treatment-to-reduce-triglycerides-and-the-risk-of-acute-pancreatitis-in-patients-with-severe-hypertriglyceridemia-sHTG/">TRYNGOLZA® (olezarsen) approved by the FDA as the first and only treatment to reduce triglycerides and the risk of acute pancreatitis in patients with severe hypertriglyceridemia (sHTG)</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced that the U.S. Food and Drug Administration (FDA) has approved TRYNGOLZA® (olezarsen) as an adjunct to diet to reduce triglycerides (TG) and the risk of acute pancreatitis in adults with severe hypertriglyceridemia (sHTG: TG greater than or equal to 500 mg/dL). TRYNGOLZA is available in a 50 mg or 80 mg...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260605705443/en/Ionis-announces-appointment-of-Ludwig-Hantson-Ph.D.-to-Board-of-Directors/">Ionis announces appointment of Ludwig Hantson, Ph.D. to Board of Directors</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced the appointment of Ludwig Hantson, Ph.D., an accomplished global biopharmaceutical leader, to the Ionis Board of Directors, effective immediately.“We are pleased to welcome Dr. Hantson to the board,” said Joseph Loscalzo, M.D., Ph.D., chairman of the Ionis Board of Directors. “Ludwig&#39;s biopharma execut...
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        <div class="me-2 text-gray">vor 6 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260527201380/en/Ionis-partner-GSK-announces-bepirovirsen-achieves-unprecedented-functional-cure-rates-with-potential-to-redefine-treatment-for-chronic-hepatitis-B/">Ionis partner GSK announces bepirovirsen achieves unprecedented functional cure rates with potential to redefine treatment for chronic hepatitis B</a>
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        CARLSBAD, Calif.--(BUSINESS WIRE)--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) partner GSK today announced positive pivotal data for bepirovirsen, an investigational antisense oligonucleotide (ASO) for the treatment of chronic hepatitis B (CHB). Results from the two Phase 3 trials, B-Well 1 and B-Well 2, were simultaneously published in the New England Journal of Medicine and presented at the Eu...
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