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   <title>Form  8-K        Inhibrx Biosciences,      For: Jun 15</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Inhibrx+Biosciences%2C++++++For%3A+Jun+15/26647343.html</link>
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   <pubDate>Mon, 15 Jun 2026 16:07:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">INBX</category>
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   <title>Form  8-K        Inhibrx Biosciences,      For: Jun 15</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Inhibrx+Biosciences%2C++++++For%3A+Jun+15/26647343.html</link>
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   <pubDate>Mon, 15 Jun 2026 16:07:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">INBX</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.21755854</category>
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   <title>Inhibrx receives FDA acceptance for ozekibart drug application</title>
   <link>http://www.streetinsider.com/Corporate+News/Inhibrx+receives+FDA+acceptance+for+ozekibart+drug+application/26645174.html</link>
   <description>&lt;p&gt;Inhibrx Biosciences Inc. (NASDAQ: INBX) announced that the U.S. Food and Drug Administration has accepted its Biologics License Application for ozekibart, a treatment for patients with unresectable or metastatic conventional chondrosarcoma.&lt;/p&gt;&lt;p&gt;The FDA set a Prescription Drug User Fee Act goal date of April 14, 2027, and identified no filing review issues. If approved, ozekibart would become the first FDA-approved treatment for this form of bone cancer.&lt;/p&gt;&lt;p&gt;The application is supported by results from the ChonDRAgon study, a randomized, placebo-controlled trial involving 206 patients across 67 sites worldwide. The study met its primary endpoint, showing ozekibart achieved a 52% reduction in risk</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:35 -0400</pubDate>
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   <title>Inhibrx receives FDA acceptance for ozekibart drug application</title>
   <link>http://www.streetinsider.com/FDA/Inhibrx+receives+FDA+acceptance+for+ozekibart+drug+application/26645174.html</link>
   <description>&lt;p&gt;Inhibrx Biosciences Inc. (NASDAQ: INBX) announced that the U.S. Food and Drug Administration has accepted its Biologics License Application for ozekibart, a treatment for patients with unresectable or metastatic conventional chondrosarcoma.&lt;/p&gt;&lt;p&gt;The FDA set a Prescription Drug User Fee Act goal date of April 14, 2027, and identified no filing review issues. If approved, ozekibart would become the first FDA-approved treatment for this form of bone cancer.&lt;/p&gt;&lt;p&gt;The application is supported by results from the ChonDRAgon study, a randomized, placebo-controlled trial involving 206 patients across 67 sites worldwide. The study met its primary endpoint, showing ozekibart achieved a 52% reduction in risk</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:35 -0400</pubDate>
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   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.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;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.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;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/Press+Releases/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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  <item>
   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/PRNewswire/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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  <item>
   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/PRNewswire/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   	  </item>
  <item>
   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/PRNewswire/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;ul type=&quot;disc&quot;&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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  <item>
   <title>Inhibrx Announces U.S. FDA Acceptance of BLA for Ozekibart in Patients with Conventional Chondrosarcoma</title>
   <link>http://www.streetinsider.com/PRNewswire/Inhibrx+Announces+U.S.+FDA+Acceptance+of+BLA+for+Ozekibart+in+Patients+with+Conventional+Chondrosarcoma/26645164.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;b&gt;&lt;i&gt;No filing review issues identified by FDA with PDUFA goal date set for &lt;chron&gt;April 14, 2027&lt;/chron&gt;&lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;li&gt;&lt;b&gt;&lt;i&gt;If Approved, Ozekibart Would Be the First and Only FDA-Approved Treatment for Unresectable or Metastatic Conventional Chondrosarcoma &lt;/i&gt;&lt;/b&gt;&lt;/li&gt;&lt;/ul&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx Biosciences, Inc.&lt;/span&gt; (Nasdaq: INBX) (&quot;&lt;span value=&quot;NASDAQ-NMS:INBX&quot; idsrc=&quot;xmltag.org&quot; &gt;Inhibrx&lt;/span&gt;&quot; or the &quot;Company&quot;), a clinical-stage biopharmaceutical company focused on developing novel biologic therapeutic candidates, today announced that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has accepted for filing its Biologics License Application (BLA) seeking approval of ozekibart (INBRX-109) for</description>
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   <pubDate>Mon, 15 Jun 2026 09:15:00 -0400</pubDate>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: MANHARD KIMBERLY</title>
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   <pubDate>Thu, 04 Jun 2026 17:29:00 -0400</pubDate>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: MANHARD KIMBERLY</title>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: FORSYTH DOUGLAS</title>
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   <pubDate>Thu, 04 Jun 2026 17:29:00 -0400</pubDate>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: FORSYTH DOUGLAS</title>
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   <pubDate>Thu, 04 Jun 2026 17:29:00 -0400</pubDate>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: Kayyem Jon Faiz</title>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: Kayyem Jon Faiz</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Inhibrx+Biosciences%2C++++++For%3A+Jun+03++Filed+by%3A+Kayyem+Jon+Faiz/26606919.html</link>
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   <pubDate>Thu, 04 Jun 2026 17:29:00 -0400</pubDate>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: Vuori Kristiina MD</title>
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   <title>Form  4          Inhibrx Biosciences,      For: Jun 03  Filed by: Vuori Kristiina MD</title>
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   <title>Form  8-K        Inhibrx Biosciences,      For: Jun 03</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Inhibrx+Biosciences%2C++++++For%3A+Jun+03/26598680.html</link>
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   <pubDate>Wed, 03 Jun 2026 16:02:00 -0400</pubDate>
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   <title>Form  8-K        Inhibrx Biosciences,      For: Jun 03</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Inhibrx+Biosciences%2C++++++For%3A+Jun+03/26598680.html</link>
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   <pubDate>Wed, 03 Jun 2026 16:02:00 -0400</pubDate>
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   <title>Inhibrx Biosciences (INBX) Reiterated at Buy by Stifel After Ozekibart Data Presentation</title>
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   <description>&lt;p&gt;Stifel analyst Dara Azar reiterated a Buy rating and $325.00 price target on Inhibrx Biosciences (NASDAQ: INBX).&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;Over the weekend at ASCO26, two Ozekibart posters were presented featuring previously disclosed data in Chondrosarcoma and Colorectal Cancer (CRC) with new granularity mainly on secondary/safety endpoints and presenter commentary. Most incremental for our CRC thesis here was the newly disclosed 11.1m single-agent response durability in Chondrosarcoma, caveated by a small responder sample, that doubles the toplined 5.5m mPFS and is likely a signal of mechanism durability in future earlier-line CRC combinations. This is important because more complex combinations become easier</description>
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   <pubDate>Tue, 02 Jun 2026 07:10:13 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  Inhibrx Biosciences,                   Filed by: VIKING GLOBAL INVESTORS LP</title>
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   <pubDate>Fri, 15 May 2026 17:52:00 -0400</pubDate>
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   <title>Form  SCHEDULE 13G/A  Inhibrx Biosciences,                   Filed by: VIKING GLOBAL INVESTORS LP</title>
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