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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
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  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
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   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</guid>
   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</guid>
   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</guid>
   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus' NDA resubmission for CAM2029 in acromegaly accepted for review by the US FDA</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;i&gt;PDUFA target action date set to &lt;chron&gt;18 December 2026&lt;/chron&gt;&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 17, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus&lt;/span&gt; (NASDAQ STO: CAMX) today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;US Food and Drug Administration&lt;/span&gt; (FDA) has accepted for review the resubmission of the New Drug Application (NDA) for CAM2029, octreotide extended-release injection, for the treatment of patients with acromegaly. The FDA has assigned a Prescription Drug User Fee Act (PDUFA) target action date of &lt;chron&gt;18 December 2026&lt;/chron&gt;.&lt;/p&gt;
&lt;p&gt;The resubmission follows the Complete Response Letter (CRL) issued by the FDA on &lt;chron&gt;10 June 2026&lt;/chron&gt;, which related</description>
   <guid isPermaLink="true">http://www.streetinsider.com/PRNewswire/Camurus%27+NDA+resubmission+for+CAM2029+in+acromegaly+accepted+for+review+by+the+US+FDA/26781059.html</guid>
   <pubDate>Fri, 17 Jul 2026 01:22:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>Camurus (CAMX) announces expansion of Lilly collaboration, decision extends Lilly's exclusive, global rights to Camurus' FluidCrystal technology</title>
   <link>http://www.streetinsider.com/General+News/Camurus+%28CAMX%29+announces+expansion+of+Lilly+collaboration%2C+decision+extends+Lilly%27s+exclusive%2C+global+rights+to+Camurus%27+FluidCrystal+technology/26581310.html</link>
   <description>&lt;p&gt;Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot;&gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon receptor agonists, and amylin receptor agonists.&lt;/p&gt;&lt;p&gt;&quot;Lilly's decision to exercise the option validates our</description>
   <guid isPermaLink="true">http://www.streetinsider.com/General+News/Camurus+%28CAMX%29+announces+expansion+of+Lilly+collaboration%2C+decision+extends+Lilly%27s+exclusive%2C+global+rights+to+Camurus%27+FluidCrystal+technology/26581310.html</guid>
   <pubDate>Mon, 01 Jun 2026 11:35:58 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">LLY</category>
   	  </item>
  <item>
   <title>Camurus (CAMX) announces expansion of Lilly collaboration, decision extends Lilly's exclusive, global rights to Camurus' FluidCrystal technology</title>
   <link>http://www.streetinsider.com/General+News/Camurus+%28CAMX%29+announces+expansion+of+Lilly+collaboration%2C+decision+extends+Lilly%27s+exclusive%2C+global+rights+to+Camurus%27+FluidCrystal+technology/26581310.html</link>
   <description>&lt;p&gt;Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot;&gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon receptor agonists, and amylin receptor agonists.&lt;/p&gt;&lt;p&gt;&quot;Lilly's decision to exercise the option validates our</description>
   <guid isPermaLink="true">http://www.streetinsider.com/General+News/Camurus+%28CAMX%29+announces+expansion+of+Lilly+collaboration%2C+decision+extends+Lilly%27s+exclusive%2C+global+rights+to+Camurus%27+FluidCrystal+technology/26581310.html</guid>
   <pubDate>Mon, 01 Jun 2026 11:35:58 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">LLY</category>
   	  </item>
  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	  </item>
  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	  </item>
  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
   	  </item>
  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
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  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/Press+Releases/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
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  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
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  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
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  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CAMX</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.01705570</category>
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  <item>
   <title>Camurus announces expansion of Lilly collaboration</title>
   <link>http://www.streetinsider.com/PRNewswire/Camurus+announces+expansion+of+Lilly+collaboration/26581302.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/se..lund&quot; idsrc=&quot;xmltag.org&quot; &gt;LUND, Sweden&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 1, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- Camurus (NASDAQ STO: CAMX) today announced that Eli Lilly and Company (&quot;Lilly&quot;) has exercised its option to include amylin receptor agonists (amylin) in the collaboration and license agreement entered in &lt;chron&gt;June 2025&lt;/chron&gt;. The decision extends Lilly's exclusive, global rights to &lt;span value=&quot;Stockholm:CAMX&quot; idsrc=&quot;xmltag.org&quot; &gt;Camurus'&lt;/span&gt; FluidCrystal&lt;sup&gt;®&lt;/sup&gt; technology for the development and commercialization of long acting cardiometabolic drug medicines to an additional compound class.&lt;/p&gt;
&lt;p&gt;The agreement comprises up to four proprietary Lilly drug compounds across three classes: dual &lt;span&gt;GLP-1&lt;/span&gt; and GIP and receptor agonists, triple agonists for &lt;span&gt;GLP-1&lt;/span&gt;, GIP and glucagon</description>
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   <pubDate>Mon, 01 Jun 2026 11:33:00 -0400</pubDate>
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