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   <title>Allergan Aesthetics Unveils the Layered Beauty Report, Advancing the Global Conversation Around Aesthetic Care</title>
   <link>http://www.streetinsider.com/Press+Releases/Allergan+Aesthetics+Unveils+the+Layered+Beauty+Report%2C+Advancing+the+Global+Conversation+Around+Aesthetic+Care/27015888.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Building on insights from the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Aesthetics Evolution series, including What Consumers Really Want, new global report explores evolving consumer attitudes toward beauty and aesthetic treatments&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 2, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Allergan Aesthetics, an &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; company, today unveiled the &lt;i&gt;Layered Beauty: The New Aesthetic Mindset&lt;/i&gt; report, informed by research among more than 12,000 beauty-involved consumers across nine global markets, complemented by practitioner expertise and regional perspectives. The report provides a global perspective on the impact of cultural attitudes toward beauty and aging to evolve the aesthetic treatment</description>
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   <pubDate>Wed, 02 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
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  <item>
   <title>Allergan Aesthetics Unveils the Layered Beauty Report, Advancing the Global Conversation Around Aesthetic Care</title>
   <link>http://www.streetinsider.com/PRNewswire/Allergan+Aesthetics+Unveils+the+Layered+Beauty+Report%2C+Advancing+the+Global+Conversation+Around+Aesthetic+Care/27015888.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Building on insights from the &lt;location value=&quot;LC/us&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S&lt;/location&gt;. Aesthetics Evolution series, including What Consumers Really Want, new global report explores evolving consumer attitudes toward beauty and aesthetic treatments&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 2, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Allergan Aesthetics, an &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; company, today unveiled the &lt;i&gt;Layered Beauty: The New Aesthetic Mindset&lt;/i&gt; report, informed by research among more than 12,000 beauty-involved consumers across nine global markets, complemented by practitioner expertise and regional perspectives. The report provides a global perspective on the impact of cultural attitudes toward beauty and aging to evolve the aesthetic treatment</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/Allergan+Aesthetics+Unveils+the+Layered+Beauty+Report%2C+Advancing+the+Global+Conversation+Around+Aesthetic+Care/27015888.html</guid>
   <pubDate>Wed, 02 Sep 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>SkinMedica® Adds Barrier Calming Cream to its Collection of Regenerative Skincare Offerings</title>
   <link>http://www.streetinsider.com/Press+Releases/SkinMedica%C2%AE+Adds+Barrier+Calming+Cream+to+its+Collection+of+Regenerative+Skincare+Offerings/27009249.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;In clinical testing, Barrier Calming Cream improved skin barrier support and reduced skin dryness by 30% after just two weeks&lt;/i&gt;&lt;i&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;&lt;span value=&quot;ACORN:3194222114&quot; idsrc=&quot;xmltag.org&quot; &gt;SkinMedica&lt;/span&gt;&lt;/i&gt;&lt;i&gt;&lt;sup&gt;®&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;also introduces HA&lt;/i&gt;&lt;i&gt;&lt;sup&gt;5®&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Hydra Collagen Facial Mist for easy, on-the-go hydration&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.irvine&quot; idsrc=&quot;xmltag.org&quot; &gt;IRVINE, Calif.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Allergan Aesthetics, an &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot; &gt;AbbVie&lt;/span&gt; company (NYSE: ABBV), expands &lt;span value=&quot;ACORN:3194222114&quot; idsrc=&quot;xmltag.org&quot; &gt;SkinMedica's&lt;/span&gt; portfolio of regenerative skincare products with the launch of Barrier Calming Cream. The restorative moisturizer is designed to soothe skin while helping restore and fortify the delicate skin barrier.&lt;/p&gt;
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   <pubDate>Tue, 01 Sep 2026 08:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>SkinMedica® Adds Barrier Calming Cream to its Collection of Regenerative Skincare Offerings</title>
   <link>http://www.streetinsider.com/PRNewswire/SkinMedica%C2%AE+Adds+Barrier+Calming+Cream+to+its+Collection+of+Regenerative+Skincare+Offerings/27009249.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;In clinical testing, Barrier Calming Cream improved skin barrier support and reduced skin dryness by 30% after just two weeks&lt;/i&gt;&lt;i&gt;&lt;sup&gt;1&lt;/sup&gt;&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;&lt;span value=&quot;ACORN:3194222114&quot; idsrc=&quot;xmltag.org&quot; &gt;SkinMedica&lt;/span&gt;&lt;/i&gt;&lt;i&gt;&lt;sup&gt;®&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;also introduces HA&lt;/i&gt;&lt;i&gt;&lt;sup&gt;5®&lt;/sup&gt;&lt;/i&gt; &lt;i&gt;Hydra Collagen Facial Mist for easy, on-the-go hydration&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.irvine&quot; idsrc=&quot;xmltag.org&quot; &gt;IRVINE, Calif.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Allergan Aesthetics, an &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot; &gt;AbbVie&lt;/span&gt; company (NYSE: ABBV), expands &lt;span value=&quot;ACORN:3194222114&quot; idsrc=&quot;xmltag.org&quot; &gt;SkinMedica's&lt;/span&gt; portfolio of regenerative skincare products with the launch of Barrier Calming Cream. The restorative moisturizer is designed to soothe skin while helping restore and fortify the delicate skin barrier.&lt;/p&gt;
    &lt;div class=&quot;PRN_ImbeddedAssetReference&quot; id=&quot;DivAssetPlaceHolder1&quot;&gt;
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   <pubDate>Tue, 01 Sep 2026 08:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>AbbVie to Present at the Wells Fargo 21st Annual Healthcare Conference</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+to+Present+at+the+Wells+Fargo+21st+Annual+Healthcare+Conference/27001292.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 31, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) will participate in the Wells Fargo 21st Annual Healthcare Conference on &lt;chron&gt;Wednesday, September 9, 2026&lt;/chron&gt;. Management will participate in a fireside chat at &lt;chron&gt;9:15 a.m. Central time&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;A live audio webcast of the presentation will be accessible through &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s Investor Relations website at &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4760466-1&amp;amp;h=2821411968&amp;amp;u=https%3A%2F%2Finvestors.abbvie.com%2F&amp;amp;a=investors.abbvie.com&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;investors.abbvie.com&lt;/a&gt;. An archived edition of the session will be available later that day.&lt;/p&gt;&lt;p&gt;&lt;b&gt;About AbbVie&lt;/b&gt;&lt;/p&gt;&lt;p&gt;AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the</description>
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   <pubDate>Mon, 31 Aug 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>AbbVie to Present at the Wells Fargo 21st Annual Healthcare Conference</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+to+Present+at+the+Wells+Fargo+21st+Annual+Healthcare+Conference/27001292.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 31, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) will participate in the Wells Fargo 21st Annual Healthcare Conference on &lt;chron&gt;Wednesday, September 9, 2026&lt;/chron&gt;. Management will participate in a fireside chat at &lt;chron&gt;9:15 a.m. Central time&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;A live audio webcast of the presentation will be accessible through &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s Investor Relations website at &lt;a target=&quot;_blank&quot; href=&quot;https://edge.prnewswire.com/c/link/?t=0&amp;amp;l=en&amp;amp;o=4760466-1&amp;amp;h=2821411968&amp;amp;u=https%3A%2F%2Finvestors.abbvie.com%2F&amp;amp;a=investors.abbvie.com&quot; target=&quot;_blank&quot; rel=&quot;nofollow&quot;&gt;investors.abbvie.com&lt;/a&gt;. An archived edition of the session will be available later that day.&lt;/p&gt;&lt;p&gt;&lt;b&gt;About AbbVie&lt;/b&gt;&lt;/p&gt;&lt;p&gt;AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the</description>
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   <pubDate>Mon, 31 Aug 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>AbbVie seeks EMA approval for Skyrizi subcutaneous use in Crohn's</title>
   <link>http://www.streetinsider.com/Corporate+News/AbbVie+seeks+EMA+approval+for+Skyrizi+subcutaneous+use+in+Crohn%27s/26983790.html</link>
   <description>&lt;p&gt;AbbVie (NYSE: ABBV) has submitted an application to the European Medicines Agency (EMA) seeking approval for Skyrizi (risankizumab) as a subcutaneous (SC) induction treatment for adults with moderately to severely active Crohn's disease.&lt;/p&gt;&lt;p&gt;The submission is supported by data from the Phase 3 AFFIRM study (NCT06063967), a randomized, placebo-controlled, double-blind trial evaluating the efficacy and safety of risankizumab SC as an induction treatment. The study enrolled 289 patients randomized in a 2:1 ratio to risankizumab SC or placebo, with co-primary endpoints of clinical remission and endoscopic response at week 12. Approximately 65% of patients had previously failed advanced therapies.&lt;/p&gt;&lt;p&gt;Skyrizi is already</description>
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   <pubDate>Thu, 27 Aug 2026 06:00:26 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>AbbVie seeks EMA approval for Skyrizi subcutaneous use in Crohn's</title>
   <link>http://www.streetinsider.com/FDA/AbbVie+seeks+EMA+approval+for+Skyrizi+subcutaneous+use+in+Crohn%27s/26983790.html</link>
   <description>&lt;p&gt;AbbVie (NYSE: ABBV) has submitted an application to the European Medicines Agency (EMA) seeking approval for Skyrizi (risankizumab) as a subcutaneous (SC) induction treatment for adults with moderately to severely active Crohn's disease.&lt;/p&gt;&lt;p&gt;The submission is supported by data from the Phase 3 AFFIRM study (NCT06063967), a randomized, placebo-controlled, double-blind trial evaluating the efficacy and safety of risankizumab SC as an induction treatment. The study enrolled 289 patients randomized in a 2:1 ratio to risankizumab SC or placebo, with co-primary endpoints of clinical remission and endoscopic response at week 12. Approximately 65% of patients had previously failed advanced therapies.&lt;/p&gt;&lt;p&gt;Skyrizi is already</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/AbbVie+seeks+EMA+approval+for+Skyrizi+subcutaneous+use+in+Crohn%27s/26983790.html</guid>
   <pubDate>Thu, 27 Aug 2026 06:00:26 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	  </item>
  <item>
   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <pubDate>Thu, 27 Aug 2026 02:00:00 -0400</pubDate>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <pubDate>Thu, 27 Aug 2026 02:00:00 -0400</pubDate>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <pubDate>Thu, 27 Aug 2026 02:00:00 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">A.31066700</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.22422661</category>
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   <title>AbbVie Submits Regulatory Application to EMA for SKYRIZI® (risankizumab) Subcutaneous Induction for Adults with Moderately to Severely Active Crohn's Disease</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+Submits+Regulatory+Application+to+EMA+for+SKYRIZI%C2%AE+%28risankizumab%29+Subcutaneous+Induction+for+Adults+with+Moderately+to+Severely+Active+Crohn%27s+Disease/26983450.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Submission supported by data from Phase 3 pivotal AFFIRM study &lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;If approved, adult Crohn's disease patients will have an additional option for induction of risankizumab which is already approved for intravenous (IV) induction&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 27, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced that it has submitted an application to the &lt;span value=&quot;ACORN:3106670068&quot; idsrc=&quot;xmltag.org&quot; &gt;European Medicines Agency&lt;/span&gt; (EMA) seeking approval for SKYRIZI&lt;sup&gt;®&lt;/sup&gt; (risankizumab) for subcutaneous (SC) induction for the treatment of adult patients with moderately to severely active Crohn's disease (CD).&lt;/p&gt;
&lt;p&gt;The application to the EMA is supported by the recently shared</description>
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   <pubDate>Thu, 27 Aug 2026 02:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">A.31066700</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.14731390</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.22422661</category>
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  <item>
   <title>AbbVie lung cancer drug data shows high response rates at WCLC 2026</title>
   <link>http://www.streetinsider.com/FDA/AbbVie+lung+cancer+drug+data+shows+high+response+rates+at+WCLC+2026/26958498.html</link>
   <description>

&lt;p&gt;AbbVie (NYSE: ABBV) announced it is presenting clinical data from multiple investigational lung cancer programs at the 2026 World Conference on Lung Cancer (WCLC), including Phase 1b results for its PD-1/VEGF bispecific antibody ABBV-1480, developed in partnership with RemeGen.&lt;/p&gt;

&lt;p&gt;In the Phase 1b study, ABBV-1480 combined with platinum-based chemotherapy as a potential first-line treatment for advanced non-small cell lung cancer (NSCLC) showed an objective response rate of 90.0% in squamous NSCLC patients (27 of 30) and 75.9% in non-squamous NSCLC patients (22 of 29) at the 10 mg/kg dose, identified as the recommended Phase 3 dose. Common treatment-related adverse events included</description>
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   <pubDate>Fri, 21 Aug 2026 07:45:22 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.14731390</category>
   	  </item>
  <item>
   <title>AbbVie lung cancer drug data shows high response rates at WCLC 2026</title>
   <link>http://www.streetinsider.com/FDA/AbbVie+lung+cancer+drug+data+shows+high+response+rates+at+WCLC+2026/26958498.html</link>
   <description>

&lt;p&gt;AbbVie (NYSE: ABBV) announced it is presenting clinical data from multiple investigational lung cancer programs at the 2026 World Conference on Lung Cancer (WCLC), including Phase 1b results for its PD-1/VEGF bispecific antibody ABBV-1480, developed in partnership with RemeGen.&lt;/p&gt;

&lt;p&gt;In the Phase 1b study, ABBV-1480 combined with platinum-based chemotherapy as a potential first-line treatment for advanced non-small cell lung cancer (NSCLC) showed an objective response rate of 90.0% in squamous NSCLC patients (27 of 30) and 75.9% in non-squamous NSCLC patients (22 of 29) at the 10 mg/kg dose, identified as the recommended Phase 3 dose. Common treatment-related adverse events included</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/AbbVie+lung+cancer+drug+data+shows+high+response+rates+at+WCLC+2026/26958498.html</guid>
   <pubDate>Fri, 21 Aug 2026 07:45:22 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.14731390</category>
   	  </item>
  <item>
   <title>AbbVie to Present New Data at WCLC 2026 Showcasing Innovation Across Lung Cancer Pipeline</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+to+Present+New+Data+at+WCLC+2026+Showcasing+Innovation+Across+Lung+Cancer+Pipeline/26958496.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Clinical data from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s ABBV-1480 (RC148) PD-1/VEGF bispecific antibody in the frontline non-small cell lung cancer (NSCLC) setting will be presented via an oral presentation&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Additionally, new data and updates from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s telisotuzumab adizutecan (Temab-A) and ABBV-706 programs across NSCLC and small cell lung cancer (SCLC) to be shared&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Research reflects &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s strategy aimed at building a lung cancer pipeline spanning next-generation immunotherapies, targeted antibody-&lt;/i&gt;&lt;i&gt;drug conjugates (ADCs) and the potential for novel combination approaches&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 21, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced new data</description>
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   <pubDate>Fri, 21 Aug 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.14731390</category>
   	  </item>
  <item>
   <title>AbbVie to Present New Data at WCLC 2026 Showcasing Innovation Across Lung Cancer Pipeline</title>
   <link>http://www.streetinsider.com/Press+Releases/AbbVie+to+Present+New+Data+at+WCLC+2026+Showcasing+Innovation+Across+Lung+Cancer+Pipeline/26958496.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Clinical data from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s ABBV-1480 (RC148) PD-1/VEGF bispecific antibody in the frontline non-small cell lung cancer (NSCLC) setting will be presented via an oral presentation&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Additionally, new data and updates from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s telisotuzumab adizutecan (Temab-A) and ABBV-706 programs across NSCLC and small cell lung cancer (SCLC) to be shared&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Research reflects &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s strategy aimed at building a lung cancer pipeline spanning next-generation immunotherapies, targeted antibody-&lt;/i&gt;&lt;i&gt;drug conjugates (ADCs) and the potential for novel combination approaches&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 21, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced new data</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/AbbVie+to+Present+New+Data+at+WCLC+2026+Showcasing+Innovation+Across+Lung+Cancer+Pipeline/26958496.html</guid>
   <pubDate>Fri, 21 Aug 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.14731390</category>
   	  </item>
  <item>
   <title>AbbVie to Present New Data at WCLC 2026 Showcasing Innovation Across Lung Cancer Pipeline</title>
   <link>http://www.streetinsider.com/PRNewswire/AbbVie+to+Present+New+Data+at+WCLC+2026+Showcasing+Innovation+Across+Lung+Cancer+Pipeline/26958496.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;i&gt;Clinical data from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s ABBV-1480 (RC148) PD-1/VEGF bispecific antibody in the frontline non-small cell lung cancer (NSCLC) setting will be presented via an oral presentation&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Additionally, new data and updates from &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s telisotuzumab adizutecan (Temab-A) and ABBV-706 programs across NSCLC and small cell lung cancer (SCLC) to be shared&lt;/i&gt;&lt;/li&gt;&lt;li&gt;&lt;i&gt;Research reflects &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt;'s strategy aimed at building a lung cancer pipeline spanning next-generation immunotherapies, targeted antibody-&lt;/i&gt;&lt;i&gt;drug conjugates (ADCs) and the potential for novel combination approaches&lt;/i&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.il.norago&quot; idsrc=&quot;xmltag.org&quot; &gt;NORTH CHICAGO, Ill.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 21, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:ABBV&quot; idsrc=&quot;xmltag.org&quot;&gt;AbbVie&lt;/span&gt; (NYSE: ABBV) today announced new data</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/AbbVie+to+Present+New+Data+at+WCLC+2026+Showcasing+Innovation+Across+Lung+Cancer+Pipeline/26958496.html</guid>
   <pubDate>Fri, 21 Aug 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">ABBV</category>
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