<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[ASH22-Program for fremlæggelse af data på Genmabs lægemidler]]></title><description><![CDATA[<p dir="auto">Genmab Announces Multiple Abstracts to be Presented at the 64th Annual Meeting and Exposition of the American Society of Hematology (ASH)<br />
Nov 3, 2022 at 2:01 PM CET</p>
<p dir="auto">Media Release</p>
<p dir="auto">Copenhagen, Denmark, November 3, 2022</p>
<p dir="auto">Nineteen abstracts accepted, including multiple presentations on the safety and efficacy of investigational epcoritamab (DuoBody<img
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      title="®"
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    />-CD3xCD20) in a variety of treatment settings and hematologic malignancies<br />
Four oral presentations highlighting data evaluating epcoritamab for the treatment of relapsed/refractory (R/R) large B-cell lymphoma (LBCL), R/R follicular lymphoma (FL), previously untreated FL, and Richter's syndrome<br />
New data evaluating investigational medicines in Genmab's early portfolio of cancer immunotherapies will also be presented<br />
Genmab to host 2022 R&amp;D Update and ASH Data Review meeting December 12</p>
<p dir="auto">Se hele programmet for Genmab/ASH:</p>
<p dir="auto"><a href="https://ir.genmab.com/news-releases/news-release-details/genmab-announces-multiple-abstracts-be-presented-64th-annual" rel="nofollow ugc">https://ir.genmab.com/news-releases/news-release-details/genmab-announces-multiple-abstracts-be-presented-64th-annual</a></p>
]]></description><link>https://dev.proinvestor.com/forum/topic/444572/ash22-program-for-fremlggelse-af-data-p-genmabs-lgemidler</link><generator>RSS for Node</generator><lastBuildDate>Sun, 28 Jun 2026 04:12:19 GMT</lastBuildDate><atom:link href="https://dev.proinvestor.com/forum/topic/444572.rss" rel="self" type="application/rss+xml"/><pubDate>Sun, 11 Dec 2022 09:48:48 GMT</pubDate><ttl>60</ttl><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Tue, 13 Dec 2022 04:22:27 GMT]]></title><description><![CDATA[<p dir="auto">2022 R&amp;D Update and ASH Data Review Dec 12, 2022 at 8:00 PM EST Genmab hosted its 2022 R&amp;D Update and ASH Data Review on Monday, December 12, 2022.</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479620</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479620</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Tue, 13 Dec 2022 04:22:27 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Mon, 12 Dec 2022 15:12:52 GMT]]></title><description><![CDATA[<p dir="auto">Janssen Presents Efficacy and Subgroup Analyses from MAIA Study Showing Long-Term Results of DARZALEX<img
      src="https://dev.proinvestor.com/forum/assets/plugins/nodebb-plugin-emoji/emoji/android/00ae.png?v=de222e39001"
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    /> (daratumumab)-based Regimen in Newly Diagnosed, Transplant-Ineligible Multiple Myeloma</p>
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<a href="https://www.prnewswire.com/news-releases/janssen-presents-efficacy-and-subgroup-analyses-from-maia-study-showing-long-term-results-of-darzalex-daratumumab-based-regimen-in-newly-diagnosed-transplant-ineligible-multiple-myeloma-301700443.html" title="Janssen Presents Efficacy and Subgroup Analyses from MAIA Study Showing Long-Term Results of DARZALEX® (daratumumab)-based Regimen in Newly Diagnosed, Transplant-Ineligible Multiple Myeloma">
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Janssen Presents Efficacy and Subgroup Analyses from MAIA Study Showing Long-Term Results of DARZALEX® (daratumumab)-based Regimen in Newly Diagnosed, Transplant-Ineligible Multiple Myeloma
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<p class="card-text line-clamp-3">/PRNewswire/ -- The Janssen Pharmaceutical Companies of Johnson & Johnson today announced new analyses from the Phase 3 MAIA study of DARZALEX® (daratumumab)...</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479621</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479621</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Mon, 12 Dec 2022 15:12:52 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Mon, 12 Dec 2022 12:34:41 GMT]]></title><description><![CDATA[<p dir="auto">Genmab to Hold 2022 R&amp;D Update and ASH Data Review Meeting <a href="https://www.proinvestor.com/investornyt" rel="nofollow ugc">https://www.proinvestor.com/investornyt</a></p>
]]></description><link>https://dev.proinvestor.com/forum/post/9479618</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479618</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Mon, 12 Dec 2022 12:34:41 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Mon, 12 Dec 2022 11:44:22 GMT]]></title><description><![CDATA[<p dir="auto">Genmab har netop præsenteret stærke data på Annual Meeting and Exposition of the American Society of Hematology (ASH). Hør mere i denne video med Helge Larsen.</p>
<p dir="auto">Disclaimer: Dette er ikke en anbefaling om køb eller salg af aktien. Helge Larsen har aktier i Genmab.</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479617</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479617</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Mon, 12 Dec 2022 11:44:22 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Mon, 12 Dec 2022 05:15:25 GMT]]></title><description><![CDATA[<p dir="auto">Genmab præsenterer lovende data for kræfthåb på konference i USA</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479622</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479622</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Mon, 12 Dec 2022 05:15:25 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Mon, 12 Dec 2022 04:21:30 GMT]]></title><description><![CDATA[<p dir="auto">Genmab Showcases Data From Robust Development Program Evaluating Epcoritamab (DuoBody<img
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      title="®"
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    />-CD3xCD20) in Patients Across a Broad Ran</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479615</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479615</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Mon, 12 Dec 2022 04:21:30 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Sun, 11 Dec 2022 19:03:38 GMT]]></title><description><![CDATA[<p dir="auto">Talquetamab Generates High Response Rate in Hard-to-Treat Multiple Myeloma .</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479616</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479616</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Sun, 11 Dec 2022 19:03:38 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Sun, 11 Dec 2022 12:09:05 GMT]]></title><description><![CDATA[<p dir="auto">Monumen-TAL - I dismantle the ASH/ NEJM Talquetamab study ' First of the ASH 2022 video series</p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479619</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479619</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Sun, 11 Dec 2022 12:09:05 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Sun, 11 Dec 2022 09:55:25 GMT]]></title><description><![CDATA[<p dir="auto">ASH 2022: Talquetamab in Patients with Relapsed/Refractory Multiple Myeloma (RRMM): Phase 1/2 Re...</p>
<p dir="auto">Recorded @ ASH 2022 PressBriefing, December 10/ More Info from ASH @ <a href="https://oncoletter.ch" rel="nofollow ugc">https://oncoletter.ch</a></p>
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]]></description><link>https://dev.proinvestor.com/forum/post/9479610</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479610</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Sun, 11 Dec 2022 09:55:25 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Sun, 11 Dec 2022 09:51:51 GMT]]></title><description><![CDATA[<p dir="auto">Janssen Presents New Data for Talquetamab, a First-in-Class GPRC5DxCD3 Bispecific Antibody, Suggesting Durable Responses in Patients with Heavily Pretreated Multiple Myeloma</p>
<p dir="auto"><a href="https://www.janssen.com/janssen-presents-new-data-talquetamab-first-class-gprc5dxcd3-bispecific-antibody-suggesting-durable" rel="nofollow ugc">https://www.janssen.com/janssen-presents-new-data-talquetamab-first-class-gprc5dxcd3-bispecific-antibody-suggesting-durable</a></p>
]]></description><link>https://dev.proinvestor.com/forum/post/9479611</link><guid isPermaLink="true">https://dev.proinvestor.com/forum/post/9479611</guid><dc:creator><![CDATA[ProinvestorNEWS]]></dc:creator><pubDate>Sun, 11 Dec 2022 09:51:51 GMT</pubDate></item><item><title><![CDATA[Reply to ASH22-Program for fremlæggelse af data på Genmabs lægemidler on Sun, 11 Dec 2022 09:50:07 GMT]]></title><description><![CDATA[<p dir="auto">Janssen Presents First Data fromMajesTEC-2 Trial of TECVAYLI (teclistamab-cqyv) in Combination with DARZALEX FASPRO (daratumumab and hyaluronidase-fihj) and Lenalidomide in Relapsed or Refractory Multiple Myeloma</p>
<p dir="auto"><a href="https://www.janssen.com/janssen-presents-first-data-majestec-2-trial-tecvayli-teclistamab-cqyv-combination-darzalex-faspro" rel="nofollow ugc">https://www.janssen.com/janssen-presents-first-data-majestec-2-trial-tecvayli-teclistamab-cqyv-combination-darzalex-faspro</a></p>
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