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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Incyte-US45337C1027">Incyte</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260507606978/en/Incyte-Announces-24-Week-Long-Term-Data-from-Phase-3-TRuE-AD4-Trial-of-Opzelura%C2%AE-ruxolitinib-Cream-in-Adults-with-Moderate-Atopic-Dermatitis/">Incyte Announces 24-Week Long-Term Data from Phase 3 TRuE-AD4 Trial of Opzelura® (ruxolitinib) Cream in Adults with Moderate Atopic Dermatitis</a>
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        WILMINGTON, Del.--(BUSINESS WIRE)--Incyte (Nasdaq:INCY) today announced final 24-week data from the Phase 3 TRuE-AD4 study evaluating the efficacy and safety of Opzelura® (ruxolitinib) cream in adults with moderate atopic dermatitis (AD) who had an inadequate response, intolerance or contraindication to topical corticosteroids (TCSs) and topical calcineurin inhibitors (TCIs). These data were pr...
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260506540858/en/Incyte-Reports-Inducement-Grants-Under-Nasdaq-Listing-Rule-5635-c-4/">Incyte Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)</a>
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        WILMINGTON, Del.--(BUSINESS WIRE)---- $INCY--Incyte Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4).
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      <a target="_blank" rel="nofollow" href="https://www.businesswire.com/news/home/20260501334677/en/Incyte-Announces-FDA-Approval-of-Jakafi-XR%E2%84%A2-ruxolitinib-Extended-Release-Tablets-for-the-Treatment-of-Myelofibrosis-Polycythemia-Vera-and-Graft-Versus-Host-Disease/">Incyte Announces FDA Approval of Jakafi XR™ (ruxolitinib) Extended-Release Tablets for the Treatment of Myelofibrosis, Polycythemia Vera and Graft-Versus-Host Disease</a>
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        WILMINGTON, Del.--(BUSINESS WIRE)--Incyte (Nasdaq:INCY) today announced that the U.S. Food and Drug Administration (FDA) has approved Jakafi XR™ (ruxolitinib) extended-release tablets for the treatment of adults with intermediate- or high-risk myelofibrosis (MF); adults with polycythemia vera (PV) who have had an inadequate response to or are intolerant of hydroxyurea; as well as adults and chi...
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