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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Pieris-Pharmaceuticals-Inc-US7207951036">Pieris Pharmaceuticals, Inc.</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/20/3298897/0/en/Palvella-Therapeutics-Presents-New-SELVA-and-TOIVA-Data-at-the-2026-International-Society-for-the-Study-of-Vascular-Anomalies-World-Congress-Supporting-QTORIN-Rapamycin-as-a-Potent.html">Palvella Therapeutics Presents New SELVA and TOIVA Data at the 2026 International Society for the Study of Vascular Anomalies World Congress Supporting QTORIN™ Rapamycin as a Potential First-in-Disease Therapy for Multiple Serious, Rare Vascular Malformations</a>
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        In SELVA Phase 3 study, 100% of participants (13/13) aged 6–11 years were rated as “Much Improved” (+2) or “Very Much Improved” (+3) on the Microcystic Lymphatic Malformation Investigator Global Assessment (mLM-IGA) scale at Week 24, with a mean improvement of +2.46 (p
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Pieris-Pharmaceuticals-Inc-US7207951036">Pieris Pharmaceuticals, Inc.</a></div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/15/3295760/0/en/palvella-therapeutics-announces-new-data-from-the-phase-2-toiva-trial-of-qtorin-rapamycin-in-cutaneous-venous-malformations-presented-at-the-83rd-annual-meeting-of-the-society-for-.html">Palvella Therapeutics Announces New Data from the Phase 2 TOIVA Trial of QTORIN™ Rapamycin in Cutaneous Venous Malformations Presented at the 83rd Annual Meeting of the Society for Investigative Dermatology</a>
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        100% of patients with bleeding at baseline demonstrated a statistically significant improvement on the Cutaneous Venous Malformations Investigator Global Assessment Bleeding scale (cVM-IGA Bleeding) at Week 12 (+2.5 point improvement; p=0.003) 100% of patients with bleeding at baseline reported being &quot;satisfied&quot; or &quot;very satisfied&quot; with QTORIN™ rapamycin on the overall satisfaction item of the ...
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/13/3293886/0/en/Palvella-Therapeutics-Announces-Uplisting-to-the-Nasdaq-Global-Market.html">Palvella Therapeutics Announces Uplisting to the Nasdaq Global Market</a>
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        Uplisting reflects Palvella&#39;s continued progress advancing potential first-in-disease therapies for serious, rare skin diseases and vascular malformations
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      <a target="_blank" rel="nofollow" href="https://www.marketbeat.com/instant-alerts/palvella-therapeutics-q1-earnings-call-highlights-2026-05-08/?utm_source=snapi">Palvella Therapeutics Q1 Earnings Call Highlights</a>
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        Palvella Therapeutics NASDAQ: PVLA said it remains on track to submit a New Drug Application in the second half of 2026 for QTORIN rapamycin in Microcystic Lymphatic Malformations, after reporting what executives described as positive Phase 3 results and outlining an expanded commercial plan supported by a recent $230 million financing.
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        <div class="text-gray">vor etwa 2 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://seekingalpha.com/article/4901109-palvella-therapeutics-inc-pvla-q1-2026-earnings-call-transcript">Palvella Therapeutics, Inc. (PVLA) Q1 2026 Earnings Call Transcript</a>
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        Palvella Therapeutics, Inc. (PVLA) Q1 2026 Earnings Call Transcript
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/07/3289863/0/en/palvella-therapeutics-reports-first-quarter-2026-financial-results-and-provides-corporate-update.html">Palvella Therapeutics Reports First Quarter 2026 Financial Results and Provides Corporate Update</a>
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        FDA Pre-New Drug Application (NDA) meeting granted for QTORIN™ rapamycin for the treatment of microcystic lymphatic malformations, with meeting expected in second quarter of 2026; NDA submission on track for second half of 2026 Accelerating U.S. launch readiness for QTORIN™ rapamycin for microcystic lymphatic malformations; BEYONDmLM.com disease awareness campaign launched to educate, engage, a...
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        <div class="text-gray">vor 2 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/04/3286595/0/en/Palvella-Therapeutics-Announces-First-Patients-Dosed-in-Phase-2-LOTU-Trial-of-Fast-Track-Designated-QTORIN-Rapamycin-for-Clinically-Significant-Angiokeratomas.html">Palvella Therapeutics Announces First Patients Dosed in Phase 2 LOTU Trial of Fast Track-Designated QTORIN™ Rapamycin for Clinically Significant Angiokeratomas</a>
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        Clinically significant angiokeratomas represent a rare, chronic and debilitating lymphatic malformation with no FDA-approved therapies and an estimated more than 50,000 diagnosed patients in the U.S.
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/04/30/3284733/0/en/Palvella-Therapeutics-to-Host-First-Quarter-2026-Financial-Results-and-Corporate-Update-Conference-Call-on-May-7-2026.html">Palvella Therapeutics to Host First Quarter 2026 Financial Results and Corporate Update Conference Call on May 7, 2026</a>
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      <div class="me-0 me-md-5">
        WAYNE, Pa., April 30, 2026 (GLOBE NEWSWIRE) -- Palvella Therapeutics, Inc. (Palvella or “the Company”) (Nasdaq: PVLA), a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapies to treat patients suffering from serious, rare skin diseases and vascular malformations for which there are no U.S. Food and Drug Administration (FDA)-approved therapies, today ...
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