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   <title>Nuvation Bio to Participate in Upcoming Investor Conferences</title>
   <link>http://www.streetinsider.com/Press+Releases/Nuvation+Bio+to+Participate+in+Upcoming+Investor+Conferences/27018904.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.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 2, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, today announced that &lt;person&gt;David Hung&lt;/person&gt;, M.D., Founder, President, and Chief Executive Officer of &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio&lt;/span&gt;, and &lt;person&gt;Philippe Sauvage&lt;/person&gt;, Chief Financial Officer of &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio&lt;/span&gt;, will participate in fireside chats and one-on-one meetings at the following conferences:&lt;/p&gt;
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   <pubDate>Wed, 02 Sep 2026 16:05:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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  <item>
   <title>Nuvation Bio to Participate in Upcoming Investor Conferences</title>
   <link>http://www.streetinsider.com/PRNewswire/Nuvation+Bio+to+Participate+in+Upcoming+Investor+Conferences/27018904.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.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Sept. 2, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, today announced that &lt;person&gt;David Hung&lt;/person&gt;, M.D., Founder, President, and Chief Executive Officer of &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio&lt;/span&gt;, and &lt;person&gt;Philippe Sauvage&lt;/person&gt;, Chief Financial Officer of &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio&lt;/span&gt;, will participate in fireside chats and one-on-one meetings at the following conferences:&lt;/p&gt;
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                &lt;p&gt;
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   <pubDate>Wed, 02 Sep 2026 16:05:00 -0400</pubDate>
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   <title>Form  4          Nuvation Bio Inc.         For: Aug 19  Filed by: Hattersley Gary</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Nuvation+Bio+Inc.+++++++++For%3A+Aug+19++Filed+by%3A+Hattersley+Gary/26962072.html</link>
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   <pubDate>Fri, 21 Aug 2026 16:50:00 -0400</pubDate>
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   <title>Form  4          Nuvation Bio Inc.         For: Aug 19  Filed by: Hattersley Gary</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Nuvation+Bio+Inc.+++++++++For%3A+Aug+19++Filed+by%3A+Hattersley+Gary/26962072.html</link>
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   <pubDate>Fri, 21 Aug 2026 16:50:00 -0400</pubDate>
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   <title>Cantor Fitzgerald Starts Nuvation Bio Inc (NUVB) at Overweight</title>
   <link>http://www.streetinsider.com/New+Coverage/Cantor+Fitzgerald+Starts+Nuvation+Bio+Inc+%28NUVB%29+at+Overweight/26958164.html</link>
   <description>(Updated - August 21, 2026 6:05 AM EDT)

&lt;p&gt;Cantor Fitzgerald analyst Li Watsek initiates coverage on Nuvation Bio Inc (NYSE: NUVB) with a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We initiate coverage of Nuvation Bio (NUVB) at Overweight. Nuvation is a low-risk, high-reward commercial-stage oncology story built on two best-in-class targeted therapies. We believe the Street materially undervalues the size of both markets, driven in part by multi-year treatment duration. Ibtrozi (taletrectinib), a next-generation ROS1 inhibitor launched in 2025, provides the valuation floor. We believe growing 1L use in ROS1+ NSCLC (non-small cell lung cancer) and a multi-year duration of therapy should drive</description>
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   <pubDate>Fri, 21 Aug 2026 06:05:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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   <title>Cantor Fitzgerald Starts Nuvation Bio Inc (NUVB) at Overweight</title>
   <link>http://www.streetinsider.com/Analyst+Comments/Cantor+Fitzgerald+Starts+Nuvation+Bio+Inc+%28NUVB%29+at+Overweight/26958164.html</link>
   <description>(Updated - August 21, 2026 6:05 AM EDT)

&lt;p&gt;Cantor Fitzgerald analyst Li Watsek initiates coverage on Nuvation Bio Inc (NYSE: NUVB) with a Overweight rating.&lt;/p&gt;&lt;p&gt;The analyst comments &quot;We initiate coverage of Nuvation Bio (NUVB) at Overweight. Nuvation is a low-risk, high-reward commercial-stage oncology story built on two best-in-class targeted therapies. We believe the Street materially undervalues the size of both markets, driven in part by multi-year treatment duration. Ibtrozi (taletrectinib), a next-generation ROS1 inhibitor launched in 2025, provides the valuation floor. We believe growing 1L use in ROS1+ NSCLC (non-small cell lung cancer) and a multi-year duration of therapy should drive</description>
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   <pubDate>Fri, 21 Aug 2026 06:05:35 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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   <title>FDA grants Nuvation Bio fast track status for brain cancer drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+grants+Nuvation+Bio+fast+track+status+for+brain+cancer+drug/26953164.html</link>
   <description>

&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) announced that the U.S. Food and Drug Administration has granted Fast Track Designation to safusidenib, the company's investigational oral drug candidate for the treatment of IDH1-mutant glioma.&lt;/p&gt;

&lt;p&gt;The designation, granted in August 2026, is intended to facilitate development and expedite the review of drugs that treat serious conditions with unmet medical need. It allows for more frequent FDA interactions during development and, if relevant criteria are met, may permit rolling review of a marketing application.&lt;/p&gt;

&lt;p&gt;The FDA's decision was based on clinical data from Nuvation Bio's safusidenib program. In the Phase 2 J201 study, at a median</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:31 -0400</pubDate>
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   <title>FDA grants Nuvation Bio fast track status for brain cancer drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+grants+Nuvation+Bio+fast+track+status+for+brain+cancer+drug/26953164.html</link>
   <description>

&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) announced that the U.S. Food and Drug Administration has granted Fast Track Designation to safusidenib, the company's investigational oral drug candidate for the treatment of IDH1-mutant glioma.&lt;/p&gt;

&lt;p&gt;The designation, granted in August 2026, is intended to facilitate development and expedite the review of drugs that treat serious conditions with unmet medical need. It allows for more frequent FDA interactions during development and, if relevant criteria are met, may permit rolling review of a marketing application.&lt;/p&gt;

&lt;p&gt;The FDA's decision was based on clinical data from Nuvation Bio's safusidenib program. In the Phase 2 J201 study, at a median</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:31 -0400</pubDate>
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   <title>FDA grants Nuvation Bio fast track status for brain cancer drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+grants+Nuvation+Bio+fast+track+status+for+brain+cancer+drug/26953164.html</link>
   <description>

&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) announced that the U.S. Food and Drug Administration has granted Fast Track Designation to safusidenib, the company's investigational oral drug candidate for the treatment of IDH1-mutant glioma.&lt;/p&gt;

&lt;p&gt;The designation, granted in August 2026, is intended to facilitate development and expedite the review of drugs that treat serious conditions with unmet medical need. It allows for more frequent FDA interactions during development and, if relevant criteria are met, may permit rolling review of a marketing application.&lt;/p&gt;

&lt;p&gt;The FDA's decision was based on clinical data from Nuvation Bio's safusidenib program. In the Phase 2 J201 study, at a median</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:31 -0400</pubDate>
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   <title>FDA grants Nuvation Bio fast track status for brain cancer drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+grants+Nuvation+Bio+fast+track+status+for+brain+cancer+drug/26953164.html</link>
   <description>

&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) announced that the U.S. Food and Drug Administration has granted Fast Track Designation to safusidenib, the company's investigational oral drug candidate for the treatment of IDH1-mutant glioma.&lt;/p&gt;

&lt;p&gt;The designation, granted in August 2026, is intended to facilitate development and expedite the review of drugs that treat serious conditions with unmet medical need. It allows for more frequent FDA interactions during development and, if relevant criteria are met, may permit rolling review of a marketing application.&lt;/p&gt;

&lt;p&gt;The FDA's decision was based on clinical data from Nuvation Bio's safusidenib program. In the Phase 2 J201 study, at a median</description>
   <guid isPermaLink="true">http://www.streetinsider.com/FDA/FDA+grants+Nuvation+Bio+fast+track+status+for+brain+cancer+drug/26953164.html</guid>
   <pubDate>Thu, 20 Aug 2026 08:00:31 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/Press+Releases/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">A.06822034</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.48341384</category>
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  <item>
   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/Press+Releases/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/Press+Releases/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/Press+Releases/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/PRNewswire/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/PRNewswire/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/PRNewswire/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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  <item>
   <title>Nuvation Bio Granted FDA Fast Track Designation for Safusidenib for Treatment of IDH1-Mutant Glioma</title>
   <link>http://www.streetinsider.com/PRNewswire/Nuvation+Bio+Granted+FDA+Fast+Track+Designation+for+Safusidenib+for+Treatment+of+IDH1-Mutant+Glioma/26953134.html</link>
   <description>
&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Designation offers pathway to expedite regulatory review, pending positive data, and reinforces safusidenib's potential to address significant medical needs for patients with IDH1-mutant glioma &lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Pivotal Phase 3 SIGMA study enrollment underway &lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ny.nyc&quot; idsrc=&quot;xmltag.org&quot; &gt;NEW YORK&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;Aug. 20, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;NYSE:NUVB&quot; idsrc=&quot;xmltag.org&quot; &gt;Nuvation Bio Inc.&lt;/span&gt; (NYSE: NUVB), a global oncology company focused on tackling some of the toughest challenges in cancer treatment, 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; (&lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;FDA&lt;/span&gt;) has granted Fast Track Designation for safusidenib, the company's investigational, oral, brain-penetrant selective inhibitor of</description>
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   <pubDate>Thu, 20 Aug 2026 08:00:00 -0400</pubDate>
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   <title>Form  144        Nuvation Bio Inc.                      Filed by: Hattersley Gary</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++Nuvation+Bio+Inc.++++++++++++++++++++++Filed+by%3A+Hattersley+Gary/26950499.html</link>
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   <pubDate>Wed, 19 Aug 2026 16:30:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
   	   	<category domain="http://rss.financialcontent.com/stocksymbol">O.48341384</category>
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  <item>
   <title>Form  144        Nuvation Bio Inc.                      Filed by: Hattersley Gary</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++144++++++++Nuvation+Bio+Inc.++++++++++++++++++++++Filed+by%3A+Hattersley+Gary/26950499.html</link>
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   <pubDate>Wed, 19 Aug 2026 16:30:00 -0400</pubDate>
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   <title>JPMorgan Starts Nuvation Bio Inc (NUVB) at Overweight</title>
   <link>http://www.streetinsider.com/New+Coverage/JPMorgan+Starts+Nuvation+Bio+Inc+%28NUVB%29+at+Overweight/26939621.html</link>
   <description>&lt;p&gt;JPMorgan analyst Priyanka Grover initiates coverage on Nuvation Bio Inc (NYSE: NUVB) with a Overweight rating and a price target of $13.00.&lt;/p&gt;&lt;p&gt;The analyst comments: “Our positive thesis centers on 1) early commercial execution for IBTROZI (taletrectinib) in advanced ROS1+ non-small cell lung cancer (NSCLC), where the launch is showing durable and growing first-line adoption; 2) ROS1+ NSCLC is a focused, biomarker-specfic market in which first-line duration, CNS activity (importantly no CNS warnings in the product label), and genetic sequencing could make the revenue opportunity more prevalence-driven over time; and 3) an increasingly highlighted safusidenib opportunity in IDH1 mutant glioma following</description>
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   <pubDate>Tue, 18 Aug 2026 03:51:10 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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  <item>
   <title>JPMorgan Starts Nuvation Bio Inc (NUVB) at Overweight</title>
   <link>http://www.streetinsider.com/Analyst+Comments/JPMorgan+Starts+Nuvation+Bio+Inc+%28NUVB%29+at+Overweight/26939621.html</link>
   <description>&lt;p&gt;JPMorgan analyst Priyanka Grover initiates coverage on Nuvation Bio Inc (NYSE: NUVB) with a Overweight rating and a price target of $13.00.&lt;/p&gt;&lt;p&gt;The analyst comments: “Our positive thesis centers on 1) early commercial execution for IBTROZI (taletrectinib) in advanced ROS1+ non-small cell lung cancer (NSCLC), where the launch is showing durable and growing first-line adoption; 2) ROS1+ NSCLC is a focused, biomarker-specfic market in which first-line duration, CNS activity (importantly no CNS warnings in the product label), and genetic sequencing could make the revenue opportunity more prevalence-driven over time; and 3) an increasingly highlighted safusidenib opportunity in IDH1 mutant glioma following</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Analyst+Comments/JPMorgan+Starts+Nuvation+Bio+Inc+%28NUVB%29+at+Overweight/26939621.html</guid>
   <pubDate>Tue, 18 Aug 2026 03:51:10 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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  <item>
   <title>Nuvation Bio Inc (NUVB) PT Raised to $20 at RBC Capital</title>
   <link>http://www.streetinsider.com/Analyst+PT+Change/Nuvation+Bio+Inc+%28NUVB%29+PT+Raised+to+%2420+at+RBC+Capital/26887504.html</link>
   <description>RBC Capital analyst Leonid Timashev raised the price target on Nuvation Bio Inc (NYSE: NUVB) to $20.00  (from $19.00) while maintaining a Outperform rating.</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Analyst+PT+Change/Nuvation+Bio+Inc+%28NUVB%29+PT+Raised+to+%2420+at+RBC+Capital/26887504.html</guid>
   <pubDate>Fri, 07 Aug 2026 07:29:56 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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   <title>Nuvation Bio Inc. (NUVB) Misses Q2 EPS by 3c</title>
   <link>http://www.streetinsider.com/Earnings/Nuvation+Bio+Inc.+%28NUVB%29+Misses+Q2+EPS+by+3c/26878883.html</link>
   <description>&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) reported Q2 EPS of ($0.18), $0.03 worse than the analyst estimate of ($0.15). Revenue for the quarter came in at $31.69 million versus the consensus estimate of $26.69 million.&lt;/p&gt;&lt;p&gt;For earnings history and earnings-related data on Nuvation Bio Inc. (NUVB) &lt;a href=&quot;http://www.streetinsider.com/ec_earnings.php?q=NUVB&quot;&gt;click here&lt;/a&gt;.&lt;/p&gt;</description>
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   <pubDate>Thu, 06 Aug 2026 07:34:27 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">NUVB</category>
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   <title>Nuvation Bio posts $31.7M Q2 revenue, widens net loss to $62.8M</title>
   <link>http://www.streetinsider.com/Corporate+News/Nuvation+Bio+posts+%2431.7M+Q2+revenue%2C+widens+net+loss+to+%2462.8M/26878838.html</link>
   <description>&lt;p&gt;Nuvation Bio Inc. (NYSE: NUVB) reported total revenue of $31.7 million for the second quarter ended June 30, 2026, up from $4.8 million in the same period a year earlier, according to a company press release.&lt;/p&gt;&lt;p&gt;Net product revenue from U.S. sales of IBTROZI (taletrectinib), the company's ROS1 inhibitor for advanced non-small cell lung cancer, was $23.2 million, a 25% increase from the prior quarter. Collaboration and license agreements revenue was $8.5 million, compared with $3.6 million in Q2 2025. Approximately 160 new patients started on IBTROZI during the quarter, with about 85% classified as TKI-naïve, representing roughly 30% quarter-over-quarter growth</description>
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   <pubDate>Thu, 06 Aug 2026 07:31:09 -0400</pubDate>
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