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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Connect-Biopharma-Holdings-Ltd-ADR-US2075231017">Connect Biopharma Holdings Ltd - ADR</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/03/30/3264498/0/en/Rademikibart-Demonstrates-Best-in-Class-Potential-in-Phase-3-Atopic-Dermatitis-Study.html">Rademikibart Demonstrates Best-in-Class Potential in Phase 3 Atopic Dermatitis Study</a>
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        – Rademikibart achieved rapid, durable efficacy results across all key endpoints through 52 weeks, with near ‑ maximal responses achieved in ~90% of patients –
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Connect-Biopharma-Holdings-Ltd-ADR-US2075231017">Connect Biopharma Holdings Ltd - ADR</a></div>
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        <div class="me-2 text-gray">GlobeNewsWire</div>
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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.globenewswire.com/news-release/2026/03/30/3264480/0/en/Connect-Biopharma-Announces-Positive-Topline-Data-from-its-Phase-1-Study-of-Intravenous-IV-Rademikibart-in-Patients-with-Asthma-or-COPD.html">Connect Biopharma Announces Positive Topline Data from its Phase 1 Study of Intravenous (IV) Rademikibart in Patients with Asthma or COPD</a>
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        – Rademikibart administered as a single 300 mg 2-minute IV push to asthma and chronic obstructive pulmonary disease (COPD) patients produced rapid improvement in FEV 1 with many patients experiencing improvements in airway function of ≥200 mL as early as 15 minutes post-dosing –
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