<turbo-stream action="append" target="news"><template>  <div class="row mb-4 py-2 news-box">
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</a></div>
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        <div class="me-2 text-gray">GlobeNewsWire</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/06/26/3318188/0/en/Replimune-Announces-FDA-Acceptance-of-RP1-Biologics-License-Application-Resubmission-for-Advanced-Melanoma.html">Replimune Announces FDA Acceptance of RP1 Biologics License Application Resubmission for Advanced Melanoma</a>
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        WOBURN, Mass., June 26, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, announced today that the U.S. Food and Drug Administration (FDA) has accepted for review the resubmission of the Biologics License Application (BLA) for RP1 (vusolimogene oderparepvec) in combination with niv...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</a></div>
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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.globenewswire.com/news-release/2026/05/31/3303918/0/en/Replimune-Presents-Final-First-in-Human-Data-for-RP2-in-Advanced-Solid-Tumors-During-Oral-Presentation-at-the-2026-American-Society-of-Clinical-Oncology-Annual-Meeting.html">Replimune Presents Final First-in-Human Data for RP2 in Advanced Solid Tumors During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting</a>
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        WOBURN, Mass., May 31, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today presented final first-in-human data for RP2 alone and in combination with nivolumab in patients with advanced solid tumors during an oral session at the 2026 American Society of Clinical Oncology annual ...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</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 4 Monaten</div>
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      <a target="_blank" rel="nofollow" href="https://www.globenewswire.com/news-release/2026/05/30/3303875/0/en/Replimune-Presents-3-Year-Landmark-Overall-Survival-Analysis-from-IGNYTE-Clinical-Trial-During-Oral-Presentation-at-the-2026-American-Society-of-Clinical-Oncology-Annual-Meeting.html">Replimune Presents 3-Year Landmark Overall Survival Analysis from IGNYTE Clinical Trial During Oral Presentation at the 2026 American Society of Clinical Oncology Annual Meeting</a>
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        WOBURN, Mass., May 30, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today presented 3-year landmark overall survival data from the IGNYTE clinical trial of RP1 plus nivolumab in patients with anti-PD-1 failed melanoma during an oral session at the 2026 American Society of Clin...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</a></div>
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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.wsj.com/health/pharma/how-replimunes-drug-got-third-chance-after-white-house-intervention-89453a87">How Replimune&#39;s drug got a third chance after the White House intervened</a>
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        Replimune representatives met with White House officials in early May and by the end of month, the Food and Drug Administration was planning to review the melanoma medication again.
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</a></div>
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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.cnbc.com/2026/05/29/replimune-resubmit-melanoma-drug-fda-makary.html">Replimune to resubmit twice-rejected drug for approval after FDA shakeup</a>
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        Replimune said it plans to resubmit its melanoma drug for approval following two earlier rejections. The move follows the departure of Food and Drug Administration Commissioner Marty Makary.
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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/replimune-reaches-agreement-with-us-fda-resubmit-melanoma-drug-application-2026-05-29/">Replimune reaches agreement with US FDA to resubmit melanoma drug application</a>
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        Replimune said ​on Friday ‌it it has reached ​an ​agreement with the ⁠U.S. ​Food and ​Drug Administration to resubmit the ​marketing ​application for its ‌experimental ⁠skin cancer drug after ​the ​regulator ⁠twice declined to ​approve ​the ⁠therapy.
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        <div class="me-2 text-gray">GlobeNewsWire</div>
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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.globenewswire.com/news-release/2026/05/29/3303541/0/en/Replimune-Announces-Planned-RP1-BLA-Resubmission-Following-Productive-Discussion-with-FDA.html">Replimune Announces Planned RP1 BLA Resubmission Following Productive Discussion with FDA</a>
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        WOBURN, Mass., May 29, 2026 (GLOBE NEWSWIRE) -- Replimune Group, Inc. (NASDAQ: REPL), a clinical-stage biotechnology company pioneering the development of novel oncolytic immunotherapies, today announced that following collaborative communications with the U.S. Food and Drug Administration (FDA), the Company and the FDA have aligned on a path forward for resubmission and reconsideration of the ...
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        <div class="me-2"><a class="text-gray" data-turbo-frame="_top" href="/aktien/Replimune-Group-Inc-US76029N1063">Replimune Group, Inc.</a></div>
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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.wsj.com/health/pharma/replimune-gets-third-try-at-fda-approval-after-makary-departure-831e07ee">Replimune Gets Third Try at FDA Approval After Makary Departure</a>
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        Experimental melanoma drug was rejected twice because the Food and Drug Administration questioned its study design.
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