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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: Jun 17</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++TuHURA+Biosciences%2C+Inc.++For%3A+Jun+17/26660390.html</link>
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   <pubDate>Wed, 17 Jun 2026 16:30:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.10076388</category>
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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: Jun 17</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++TuHURA+Biosciences%2C+Inc.++For%3A+Jun+17/26660390.html</link>
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   <pubDate>Wed, 17 Jun 2026 16:30:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.10076388</category>
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   <title>TuHURA Biosciences (HURA) Reiterated at Market Outperform by Citizens </title>
   <link>http://www.streetinsider.com/Analyst+Comments/TuHURA+Biosciences+%28HURA%29+Reiterated+at+Market+Outperform+by+Citizens+/26649597.html</link>
   <description>&lt;p&gt;Citizens analyst Silvan Turkcan reiterated a Market Outperform rating and $9.00 price target on TuHURA Biosciences (NASDAQ: HURA).&lt;/p&gt;&lt;p&gt;The analyst commented, &quot;We are encouraged to see TuHURA Biosciences kick off clinical development in the acute myeloid leukemia (AML) space, where menin inhibitors have demonstrated that significant value can be created. HURA announced the IND filing for anti-VISTA mAb, TBS-2025, after the FDA aligned with prior guidance on the development pathway for monotherapy and combination with menin inhibitors for AML. Following written responses related to the company's proposed Phase 1b/2 development plan, HURA is targeting study initiation in 2H26. We maintain our</description>
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   <pubDate>Tue, 16 Jun 2026 05:17:41 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
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  <item>
   <title>TuHURA Biosciences files IND for TBS-2025 antibody in blood cancers</title>
   <link>http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</link>
   <description>

&lt;p&gt;TuHURA Biosciences Inc. (NASDAQ: HURA) filed an Investigational New Drug application with the U.S. Food and Drug Administration for its TBS-2025 VISTA inhibiting antibody to treat molecularly defined subsets of acute myeloid leukemia and other blood-related cancers.&lt;/p&gt;

&lt;p&gt;The IND filing follows guidance from the FDA on the development pathway for both monotherapy and combination treatments with menin inhibitors for AML. The FDA indicated that a requested meeting would not be necessary and will provide written responses to questions about the company's proposed Phase 1b/2 development plan for TBS-2025 in AML.&lt;/p&gt;

&lt;p&gt;TuHURA targets initiation of the Phase 1b/2 study in the second half</description>
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   <pubDate>Mon, 15 Jun 2026 07:49:38 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.10076388</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
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   <title>TuHURA Biosciences files IND for TBS-2025 antibody in blood cancers</title>
   <link>http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</link>
   <description>

&lt;p&gt;TuHURA Biosciences Inc. (NASDAQ: HURA) filed an Investigational New Drug application with the U.S. Food and Drug Administration for its TBS-2025 VISTA inhibiting antibody to treat molecularly defined subsets of acute myeloid leukemia and other blood-related cancers.&lt;/p&gt;

&lt;p&gt;The IND filing follows guidance from the FDA on the development pathway for both monotherapy and combination treatments with menin inhibitors for AML. The FDA indicated that a requested meeting would not be necessary and will provide written responses to questions about the company's proposed Phase 1b/2 development plan for TBS-2025 in AML.&lt;/p&gt;

&lt;p&gt;TuHURA targets initiation of the Phase 1b/2 study in the second half</description>
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   <pubDate>Mon, 15 Jun 2026 07:49:38 -0400</pubDate>
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   <title>TuHURA Biosciences files IND for TBS-2025 antibody in blood cancers</title>
   <link>http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</link>
   <description>

&lt;p&gt;TuHURA Biosciences Inc. (NASDAQ: HURA) filed an Investigational New Drug application with the U.S. Food and Drug Administration for its TBS-2025 VISTA inhibiting antibody to treat molecularly defined subsets of acute myeloid leukemia and other blood-related cancers.&lt;/p&gt;

&lt;p&gt;The IND filing follows guidance from the FDA on the development pathway for both monotherapy and combination treatments with menin inhibitors for AML. The FDA indicated that a requested meeting would not be necessary and will provide written responses to questions about the company's proposed Phase 1b/2 development plan for TBS-2025 in AML.&lt;/p&gt;

&lt;p&gt;TuHURA targets initiation of the Phase 1b/2 study in the second half</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</guid>
   <pubDate>Mon, 15 Jun 2026 07:49:38 -0400</pubDate>
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   <title>TuHURA Biosciences files IND for TBS-2025 antibody in blood cancers</title>
   <link>http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</link>
   <description>

&lt;p&gt;TuHURA Biosciences Inc. (NASDAQ: HURA) filed an Investigational New Drug application with the U.S. Food and Drug Administration for its TBS-2025 VISTA inhibiting antibody to treat molecularly defined subsets of acute myeloid leukemia and other blood-related cancers.&lt;/p&gt;

&lt;p&gt;The IND filing follows guidance from the FDA on the development pathway for both monotherapy and combination treatments with menin inhibitors for AML. The FDA indicated that a requested meeting would not be necessary and will provide written responses to questions about the company's proposed Phase 1b/2 development plan for TBS-2025 in AML.&lt;/p&gt;

&lt;p&gt;TuHURA targets initiation of the Phase 1b/2 study in the second half</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/TuHURA+Biosciences+files+IND+for+TBS-2025+antibody+in+blood+cancers/26644300.html</guid>
   <pubDate>Mon, 15 Jun 2026 07:49:38 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   	  </item>
  <item>
   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</guid>
   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</guid>
   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</guid>
   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.10076388</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.20026344</category>
   	  </item>
  <item>
   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
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   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">HURA</category>
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   	  </item>
  <item>
   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/PRNewswire/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
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   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
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   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/PRNewswire/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
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   <pubDate>Mon, 15 Jun 2026 07:45:00 -0400</pubDate>
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   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/PRNewswire/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
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   <title>TuHURA Biosciences Files Investigational New Drug Application for Evaluation of the TBS-2025 VISTA Inhibiting Antibody in Molecularly Defined Subsets of AML and Other Blood Related Cancers</title>
   <link>http://www.streetinsider.com/PRNewswire/TuHURA+Biosciences+Files+Investigational+New+Drug+Application+for+Evaluation+of+the+TBS-2025+VISTA+Inhibiting+Antibody+in+Molecularly+Defined+Subsets+of+AML+and+Other+Blood+Related+Cancers/26644298.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The IND is aligned with guidance previously provided by the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) on the development pathway for both monotherapy and combination with menin inhibitors for &lt;/i&gt;Acute Myeloid Leukemia (AML)&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The FDA noted that the requested meeting would not be necessary and that it will instead provide written responses to questions and information related to the Company's proposed Phase 1b/2 development plan for TBS-2025 in AML &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;The Company is targeting initiation of the Phase 1b/2 study in the second half of 2026&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&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;</description>
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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: May 26</title>
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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: May 26</title>
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   <title>Form  4          TuHURA Biosciences, Inc.  For: May 28  Filed by: Bianco James A.</title>
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   <pubDate>Fri, 29 May 2026 16:37:00 -0400</pubDate>
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   <title>Form  4          TuHURA Biosciences, Inc.  For: May 28  Filed by: Bianco James A.</title>
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   <pubDate>Fri, 29 May 2026 16:37:00 -0400</pubDate>
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   <title>Form  10-Q       TuHURA Biosciences, Inc.  For: Mar 31</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++10-Q+++++++TuHURA+Biosciences%2C+Inc.++For%3A+Mar+31/26507899.html</link>
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   <pubDate>Fri, 15 May 2026 17:21:00 -0400</pubDate>
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   <title>Form  10-Q       TuHURA Biosciences, Inc.  For: Mar 31</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++10-Q+++++++TuHURA+Biosciences%2C+Inc.++For%3A+Mar+31/26507899.html</link>
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   <pubDate>Fri, 15 May 2026 17:21:00 -0400</pubDate>
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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: May 15</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++TuHURA+Biosciences%2C+Inc.++For%3A+May+15/26507757.html</link>
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   <pubDate>Fri, 15 May 2026 17:11:00 -0400</pubDate>
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   <title>Form  8-K        TuHURA Biosciences, Inc.  For: May 15</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++TuHURA+Biosciences%2C+Inc.++For%3A+May+15/26507757.html</link>
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   <pubDate>Fri, 15 May 2026 17:11:00 -0400</pubDate>
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   <title>TuHURA Biosciences Reports First Quarter 2026 Financial Results and Provides a Corporate Update</title>
   <link>http://www.streetinsider.com/Press+Releases/TuHURA+Biosciences+Reports+First+Quarter+2026+Financial+Results+and+Provides+a+Corporate+Update/26507483.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:HURA&quot; idsrc=&quot;xmltag.org&quot; &gt;TuHURA Biosciences, Inc.&lt;/span&gt; (NASDAQ: HURA) (&quot;TuHURA&quot; or the &quot;Company&quot;), a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, today reported financial results for the Company's first quarter ended &lt;chron&gt;March 31, 2026&lt;/chron&gt;, and provided a corporate update.&lt;/p&gt;&lt;p&gt;&quot;I am very pleased with the progress we have made this past quarter as we continue to execute upon our corporate and development strategy. Importantly, we recently established a &lt;money&gt;$50 million&lt;/money&gt; non-equity-based source of operating capital in the form of credit facility with our</description>
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   <pubDate>Fri, 15 May 2026 17:00:00 -0400</pubDate>
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   <title>TuHURA Biosciences Reports First Quarter 2026 Financial Results and Provides a Corporate Update</title>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.fl.tampa&quot; idsrc=&quot;xmltag.org&quot; &gt;TAMPA, Fla.&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;May 15, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NASDAQ-NMS:HURA&quot; idsrc=&quot;xmltag.org&quot; &gt;TuHURA Biosciences, Inc.&lt;/span&gt; (NASDAQ: HURA) (&quot;TuHURA&quot; or the &quot;Company&quot;), a Phase 3 immuno-oncology company developing novel therapeutics to overcome resistance to cancer immunotherapy, today reported financial results for the Company's first quarter ended &lt;chron&gt;March 31, 2026&lt;/chron&gt;, and provided a corporate update.&lt;/p&gt;&lt;p&gt;&quot;I am very pleased with the progress we have made this past quarter as we continue to execute upon our corporate and development strategy. Importantly, we recently established a &lt;money&gt;$50 million&lt;/money&gt; non-equity-based source of operating capital in the form of credit facility with our</description>
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