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   <title>CEL-SCI launches phase 3 confirmatory study for head and neck cancer drug</title>
   <link>http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it is launching a global confirmatory registration study of its investigational drug Multikine (Leukocyte Interleukin, Injection) as a neoadjuvant treatment for newly diagnosed, previously untreated, resectable, locally advanced head and neck cancer.&lt;/p&gt;

&lt;p&gt;The study will enroll approximately 212 patients across clinical centers in the United States, Europe, Asia, and South America. Orient EuroPharma, CEL-SCI's partner in Taiwan, will oversee and fund enrollment within its territory.&lt;/p&gt;

&lt;p&gt;The study targets patients with squamous cell carcinoma of the head and neck whose tumors show low or zero PD-L1 expression and no clinical lymph node involvement. This cohort reflects a</description>
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   <pubDate>Mon, 13 Jul 2026 08:01:10 -0400</pubDate>
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   <title>CEL-SCI launches phase 3 confirmatory study for head and neck cancer drug</title>
   <link>http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it is launching a global confirmatory registration study of its investigational drug Multikine (Leukocyte Interleukin, Injection) as a neoadjuvant treatment for newly diagnosed, previously untreated, resectable, locally advanced head and neck cancer.&lt;/p&gt;

&lt;p&gt;The study will enroll approximately 212 patients across clinical centers in the United States, Europe, Asia, and South America. Orient EuroPharma, CEL-SCI's partner in Taiwan, will oversee and fund enrollment within its territory.&lt;/p&gt;

&lt;p&gt;The study targets patients with squamous cell carcinoma of the head and neck whose tumors show low or zero PD-L1 expression and no clinical lymph node involvement. This cohort reflects a</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:01:10 -0400</pubDate>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
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   <title>CEL-SCI launches phase 3 confirmatory study for head and neck cancer drug</title>
   <link>http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it is launching a global confirmatory registration study of its investigational drug Multikine (Leukocyte Interleukin, Injection) as a neoadjuvant treatment for newly diagnosed, previously untreated, resectable, locally advanced head and neck cancer.&lt;/p&gt;

&lt;p&gt;The study will enroll approximately 212 patients across clinical centers in the United States, Europe, Asia, and South America. Orient EuroPharma, CEL-SCI's partner in Taiwan, will oversee and fund enrollment within its territory.&lt;/p&gt;

&lt;p&gt;The study targets patients with squamous cell carcinoma of the head and neck whose tumors show low or zero PD-L1 expression and no clinical lymph node involvement. This cohort reflects a</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:01:10 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
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  <item>
   <title>CEL-SCI launches phase 3 confirmatory study for head and neck cancer drug</title>
   <link>http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it is launching a global confirmatory registration study of its investigational drug Multikine (Leukocyte Interleukin, Injection) as a neoadjuvant treatment for newly diagnosed, previously untreated, resectable, locally advanced head and neck cancer.&lt;/p&gt;

&lt;p&gt;The study will enroll approximately 212 patients across clinical centers in the United States, Europe, Asia, and South America. Orient EuroPharma, CEL-SCI's partner in Taiwan, will oversee and fund enrollment within its territory.&lt;/p&gt;

&lt;p&gt;The study targets patients with squamous cell carcinoma of the head and neck whose tumors show low or zero PD-L1 expression and no clinical lymph node involvement. This cohort reflects a</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/CEL-SCI+launches+phase+3+confirmatory+study+for+head+and+neck+cancer+drug/26760108.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:01:10 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
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   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">CVM</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.02168038</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</guid>
   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>CEL-SCI to Launch FDA Registration-Enabling Phase 3 Confirmatory Study to Bring Multikine® to Market for Newly Diagnosed Head and Neck Cancer</title>
   <link>http://www.streetinsider.com/Business+Wire/CEL-SCI+to+Launch+FDA+Registration-Enabling+Phase+3+Confirmatory+Study+to+Bring+Multikine%C2%AE+to+Market+for+Newly+Diagnosed+Head+and+Neck+Cancer/26760011.html</link>
   <description>
&lt;ul class=&quot;bwlistdisc&quot;&gt;
&lt;li&gt;
&lt;i&gt;Patient enrollment expected to commence at clinical centers in the U.S., Europe, Asia and later on in South America&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;The 212-patient confirmatory study is powered at approximately 97% to confirm a previously observed 0.34 hazard ratio, representing a 66% reduction in the risk of death&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;In the target population, Multikine followed by standard of care increased the 5-year survival rate to 73% versus 45% with standard of care alone&lt;/i&gt;

&lt;/li&gt;
&lt;li&gt;
&lt;i&gt;Pre-surgical tumor responses will be assessed and may serve as the basis for an early conditional or accelerated approval application with the FDA&lt;/i&gt;

&lt;/li&gt;
&lt;/ul&gt;
&lt;p&gt;    VIENNA, Va.--(BUSINESS WIRE)--
CEL-SCI Corporation &lt;b&gt;(NYSE American: CVM)&lt;/b&gt;</description>
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   <pubDate>Mon, 13 Jul 2026 08:00:00 -0400</pubDate>
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   <title>Form  ARS        CEL SCI CORP              For: Sep 30</title>
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   <pubDate>Thu, 02 Jul 2026 17:08:00 -0400</pubDate>
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   <title>Form  ARS        CEL SCI CORP              For: Sep 30</title>
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   <pubDate>Thu, 02 Jul 2026 17:08:00 -0400</pubDate>
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   <title>Form  DEF 14A    CEL SCI CORP              For: Jun 23</title>
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   <pubDate>Thu, 02 Jul 2026 17:02:00 -0400</pubDate>
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   <title>Form  DEF 14A    CEL SCI CORP              For: Jun 23</title>
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   <pubDate>Thu, 02 Jul 2026 17:02:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: TALOR EYAL</title>
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   <pubDate>Wed, 01 Jul 2026 08:41:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: TALOR EYAL</title>
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   <pubDate>Wed, 01 Jul 2026 08:41:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: PRICHEP PATRICIA  B</title>
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   <pubDate>Wed, 01 Jul 2026 08:38:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: PRICHEP PATRICIA  B</title>
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   <pubDate>Wed, 01 Jul 2026 08:38:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: KERSTEN GEERT R</title>
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   <pubDate>Wed, 01 Jul 2026 08:33:00 -0400</pubDate>
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   <title>Form  4          CEL SCI CORP              For: Jun 30  Filed by: KERSTEN GEERT R</title>
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   <pubDate>Wed, 01 Jul 2026 08:33:00 -0400</pubDate>
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   <title>CEL-SCI signs distribution deal with Saudi Amarox for cancer drug</title>
   <link>http://www.streetinsider.com/Corporate+News/CEL-SCI+signs+distribution+deal+with+Saudi+Amarox+for+cancer+drug/26682377.html</link>
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&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it signed an agreement with Saudi Amarox at the BIO International Convention 2026 on June 22 in San Diego, covering regulatory, marketing, distribution, and revenue sharing for its investigational cancer therapy Multikine in Saudi Arabia.&lt;/p&gt;

&lt;p&gt;Under the agreement, Amarox will support the planned introduction and commercialization of Multikine in Saudi Arabia, with an option to extend to other Gulf Cooperation Council countries, subject to regulatory approvals. Multikine has not been approved by the FDA or any other regulatory agency, and its safety and efficacy have not been established for any use.&lt;/p&gt;

&lt;p&gt;Multikine is an investigational cancer</description>
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   <pubDate>Wed, 24 Jun 2026 08:00:34 -0400</pubDate>
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   <title>CEL-SCI signs distribution deal with Saudi Amarox for cancer drug</title>
   <link>http://www.streetinsider.com/Corporate+News/CEL-SCI+signs+distribution+deal+with+Saudi+Amarox+for+cancer+drug/26682377.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it signed an agreement with Saudi Amarox at the BIO International Convention 2026 on June 22 in San Diego, covering regulatory, marketing, distribution, and revenue sharing for its investigational cancer therapy Multikine in Saudi Arabia.&lt;/p&gt;

&lt;p&gt;Under the agreement, Amarox will support the planned introduction and commercialization of Multikine in Saudi Arabia, with an option to extend to other Gulf Cooperation Council countries, subject to regulatory approvals. Multikine has not been approved by the FDA or any other regulatory agency, and its safety and efficacy have not been established for any use.&lt;/p&gt;

&lt;p&gt;Multikine is an investigational cancer</description>
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   <pubDate>Wed, 24 Jun 2026 08:00:34 -0400</pubDate>
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   <title>CEL-SCI signs distribution deal with Saudi Amarox for cancer drug</title>
   <link>http://www.streetinsider.com/Corporate+News/CEL-SCI+signs+distribution+deal+with+Saudi+Amarox+for+cancer+drug/26682377.html</link>
   <description>

&lt;p&gt;CEL-SCI Corporation (NYSE American: CVM) announced it signed an agreement with Saudi Amarox at the BIO International Convention 2026 on June 22 in San Diego, covering regulatory, marketing, distribution, and revenue sharing for its investigational cancer therapy Multikine in Saudi Arabia.&lt;/p&gt;

&lt;p&gt;Under the agreement, Amarox will support the planned introduction and commercialization of Multikine in Saudi Arabia, with an option to extend to other Gulf Cooperation Council countries, subject to regulatory approvals. Multikine has not been approved by the FDA or any other regulatory agency, and its safety and efficacy have not been established for any use.&lt;/p&gt;

&lt;p&gt;Multikine is an investigational cancer</description>
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   <pubDate>Wed, 24 Jun 2026 08:00:34 -0400</pubDate>
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