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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Corvese Brian</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Corvese+Brian/26591547.html</link>
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   <pubDate>Tue, 02 Jun 2026 16:06:00 -0400</pubDate>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Corvese Brian</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Corvese+Brian/26591547.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Ryan Barbara</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Ryan+Barbara/26591561.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Ryan Barbara</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Ryan+Barbara/26591561.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Holcomb John Bradley</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Holcomb+John+Bradley/26591568.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Holcomb John Bradley</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Holcomb+John+Bradley/26591568.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: WIINBERG ULF</title>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: WIINBERG ULF</title>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Behner Peter</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Behner+Peter/26591541.html</link>
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   <title>Form  4          MiNK Therapeutics, Inc.   For: Mar 02  Filed by: Behner Peter</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++MiNK+Therapeutics%2C+Inc.+++For%3A+Mar+02++Filed+by%3A+Behner+Peter/26591541.html</link>
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   <title>MiNK Therapeutics doses first patient in phase 2 lung injury trial</title>
   <link>http://www.streetinsider.com/FDA/MiNK+Therapeutics+doses+first+patient+in+phase+2+lung+injury+trial/26562324.html</link>
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&lt;p&gt;MiNK Therapeutics (NASDAQ: INKT) announced that the first patient has been dosed in its randomized Phase 2 clinical trial evaluating agenT-797 for acute lung injury and critical illness.&lt;/p&gt;

&lt;p&gt;The patient was dosed at First Lviv Territorial Medical Union in Lviv, Ukraine, following approval from Ukraine's Ministry of Health. The trial, designated C-1300-02, compares agenT-797 plus standard care against placebo plus standard care in patients with acute lung injury meeting Global Acute Respiratory Distress Syndrome criteria.&lt;/p&gt;

&lt;p&gt;The study evaluates intensive care unit outcomes including survival, ventilator-free days, ICU recovery, and biological measures related to treatment activity and immune function. The company expects preliminary</description>
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   <pubDate>Thu, 28 May 2026 09:05:03 -0400</pubDate>
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   <title>MiNK Therapeutics doses first patient in phase 2 lung injury trial</title>
   <link>http://www.streetinsider.com/FDA/MiNK+Therapeutics+doses+first+patient+in+phase+2+lung+injury+trial/26562324.html</link>
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&lt;p&gt;MiNK Therapeutics (NASDAQ: INKT) announced that the first patient has been dosed in its randomized Phase 2 clinical trial evaluating agenT-797 for acute lung injury and critical illness.&lt;/p&gt;

&lt;p&gt;The patient was dosed at First Lviv Territorial Medical Union in Lviv, Ukraine, following approval from Ukraine's Ministry of Health. The trial, designated C-1300-02, compares agenT-797 plus standard care against placebo plus standard care in patients with acute lung injury meeting Global Acute Respiratory Distress Syndrome criteria.&lt;/p&gt;

&lt;p&gt;The study evaluates intensive care unit outcomes including survival, ventilator-free days, ICU recovery, and biological measures related to treatment activity and immune function. The company expects preliminary</description>
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   <title>MiNK Therapeutics doses first patient in phase 2 lung injury trial</title>
   <link>http://www.streetinsider.com/FDA/MiNK+Therapeutics+doses+first+patient+in+phase+2+lung+injury+trial/26562324.html</link>
   <description>

&lt;p&gt;MiNK Therapeutics (NASDAQ: INKT) announced that the first patient has been dosed in its randomized Phase 2 clinical trial evaluating agenT-797 for acute lung injury and critical illness.&lt;/p&gt;

&lt;p&gt;The patient was dosed at First Lviv Territorial Medical Union in Lviv, Ukraine, following approval from Ukraine's Ministry of Health. The trial, designated C-1300-02, compares agenT-797 plus standard care against placebo plus standard care in patients with acute lung injury meeting Global Acute Respiratory Distress Syndrome criteria.&lt;/p&gt;

&lt;p&gt;The study evaluates intensive care unit outcomes including survival, ventilator-free days, ICU recovery, and biological measures related to treatment activity and immune function. The company expects preliminary</description>
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   <title>MiNK Therapeutics doses first patient in phase 2 lung injury trial</title>
   <link>http://www.streetinsider.com/FDA/MiNK+Therapeutics+doses+first+patient+in+phase+2+lung+injury+trial/26562324.html</link>
   <description>

&lt;p&gt;MiNK Therapeutics (NASDAQ: INKT) announced that the first patient has been dosed in its randomized Phase 2 clinical trial evaluating agenT-797 for acute lung injury and critical illness.&lt;/p&gt;

&lt;p&gt;The patient was dosed at First Lviv Territorial Medical Union in Lviv, Ukraine, following approval from Ukraine's Ministry of Health. The trial, designated C-1300-02, compares agenT-797 plus standard care against placebo plus standard care in patients with acute lung injury meeting Global Acute Respiratory Distress Syndrome criteria.&lt;/p&gt;

&lt;p&gt;The study evaluates intensive care unit outcomes including survival, ventilator-free days, ICU recovery, and biological measures related to treatment activity and immune function. The company expects preliminary</description>
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   <pubDate>Thu, 28 May 2026 09:05:03 -0400</pubDate>
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   <title>MiNK Therapeutics Announces First Patient Dosed in Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury and Critical Illness</title>
   <link>http://www.streetinsider.com/Press+Releases/MiNK+Therapeutics+Announces+First+Patient+Dosed+in+Randomized+Phase+2+Trial+of+agenT-797+in+Acute+Lung+Injury+and+Critical+Illness/26562316.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;First patient dosed marks rapid transition from trial activation to active treatment in patients with acute lung injury from all cause pneumonia meeting Global ARDS criteria&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Landmark advances a first-in-class immune therapy for critical illness where there are no approved mortality-reducing therapies&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Preliminary data expected in the second half of 2026&lt;/em&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;NEW YORK and LVIV, Ukraine, May  28, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=BpxtMJBkReNegAiN6gJGuFzX7JpY6RkbDQku3TGn-cvPh-x4YHn_83groXgoaZKwuLff9iCxB6Kaw97z9m0JXQHzd2WNmXMY8vEvhyz0cn0=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;MiNK Therapeutics&lt;/a&gt; (NASDAQ: INKT), a clinical-stage biopharmaceutical company pioneering off-the-shelf allogeneic iNKT cell therapies for cancer and immune disorders, today announced that the first patient has been</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/MiNK+Therapeutics+Announces+First+Patient+Dosed+in+Randomized+Phase+2+Trial+of+agenT-797+in+Acute+Lung+Injury+and+Critical+Illness/26562316.html</guid>
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   <title>MiNK Therapeutics Announces First Patient Dosed in Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury and Critical Illness</title>
   <link>http://www.streetinsider.com/Press+Releases/MiNK+Therapeutics+Announces+First+Patient+Dosed+in+Randomized+Phase+2+Trial+of+agenT-797+in+Acute+Lung+Injury+and+Critical+Illness/26562316.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;First patient dosed marks rapid transition from trial activation to active treatment in patients with acute lung injury from all cause pneumonia meeting Global ARDS criteria&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Landmark advances a first-in-class immune therapy for critical illness where there are no approved mortality-reducing therapies&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Preliminary data expected in the second half of 2026&lt;/em&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;NEW YORK and LVIV, Ukraine, May  28, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=BpxtMJBkReNegAiN6gJGuFzX7JpY6RkbDQku3TGn-cvPh-x4YHn_83groXgoaZKwuLff9iCxB6Kaw97z9m0JXQHzd2WNmXMY8vEvhyz0cn0=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;MiNK Therapeutics&lt;/a&gt; (NASDAQ: INKT), a clinical-stage biopharmaceutical company pioneering off-the-shelf allogeneic iNKT cell therapies for cancer and immune disorders, today announced that the first patient has been</description>
   <guid isPermaLink="true">http://www.streetinsider.com/Press+Releases/MiNK+Therapeutics+Announces+First+Patient+Dosed+in+Randomized+Phase+2+Trial+of+agenT-797+in+Acute+Lung+Injury+and+Critical+Illness/26562316.html</guid>
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   <title>MiNK Therapeutics Announces First Patient Dosed in Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury and Critical Illness</title>
   <link>http://www.streetinsider.com/Press+Releases/MiNK+Therapeutics+Announces+First+Patient+Dosed+in+Randomized+Phase+2+Trial+of+agenT-797+in+Acute+Lung+Injury+and+Critical+Illness/26562316.html</link>
   <description>
&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;First patient dosed marks rapid transition from trial activation to active treatment in patients with acute lung injury from all cause pneumonia meeting Global ARDS criteria&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Landmark advances a first-in-class immune therapy for critical illness where there are no approved mortality-reducing therapies&lt;/em&gt;&lt;/li&gt;&lt;li style=&quot;margin-top:4pt; margin-bottom:8pt;&quot;&gt;&lt;em&gt;Preliminary data expected in the second half of 2026&lt;/em&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;NEW YORK and LVIV, Ukraine, May  28, 2026  (GLOBE NEWSWIRE) -- &lt;a target=&quot;_blank&quot; href=&quot;https://www.globenewswire.com/Tracker?data=BpxtMJBkReNegAiN6gJGuFzX7JpY6RkbDQku3TGn-cvPh-x4YHn_83groXgoaZKwuLff9iCxB6Kaw97z9m0JXQHzd2WNmXMY8vEvhyz0cn0=&quot; rel=&quot;nofollow&quot; target=&quot;_blank&quot;&gt;MiNK Therapeutics&lt;/a&gt; (NASDAQ: INKT), a clinical-stage biopharmaceutical company pioneering off-the-shelf allogeneic iNKT cell therapies for cancer and immune disorders, today announced that the first patient has been</description>
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   <title>MiNK Therapeutics Announces First Patient Dosed in Randomized Phase 2 Trial of agenT-797 in Acute Lung Injury and Critical Illness</title>
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   <description>&lt;p&gt;Agenus Inc. (NASDAQ: AGEN) announced retrospective data showing that artificial intelligence analysis of routine tumor images identified patients more likely to respond to its experimental cancer treatment combination.&lt;/p&gt;&lt;p&gt;The analysis used Noetik's TARIO-2 platform to examine standard pathology images from 113 patients treated with botensilimab plus balstilimab in a Phase 1b trial. The AI system analyzed spatial tumor microenvironment patterns from hematoxylin and eosin stained tissue samples taken before treatment.&lt;/p&gt;&lt;p&gt;In patients with microsatellite stable metastatic colorectal cancer without active liver metastases, the AI-identified subgroup showed a 64% response rate compared to 9% in the remaining patients. The AI-identified group also demonstrated</description>
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   <description>&lt;p&gt;Agenus Inc. (NASDAQ: AGEN) announced retrospective data showing that artificial intelligence analysis of routine tumor images identified patients more likely to respond to its experimental cancer treatment combination.&lt;/p&gt;&lt;p&gt;The analysis used Noetik's TARIO-2 platform to examine standard pathology images from 113 patients treated with botensilimab plus balstilimab in a Phase 1b trial. The AI system analyzed spatial tumor microenvironment patterns from hematoxylin and eosin stained tissue samples taken before treatment.&lt;/p&gt;&lt;p&gt;In patients with microsatellite stable metastatic colorectal cancer without active liver metastases, the AI-identified subgroup showed a 64% response rate compared to 9% in the remaining patients. The AI-identified group also demonstrated</description>
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   <description>&lt;p&gt;Agenus Inc. (NASDAQ: AGEN) announced retrospective data showing that artificial intelligence analysis of routine tumor images identified patients more likely to respond to its experimental cancer treatment combination.&lt;/p&gt;&lt;p&gt;The analysis used Noetik's TARIO-2 platform to examine standard pathology images from 113 patients treated with botensilimab plus balstilimab in a Phase 1b trial. The AI system analyzed spatial tumor microenvironment patterns from hematoxylin and eosin stained tissue samples taken before treatment.&lt;/p&gt;&lt;p&gt;In patients with microsatellite stable metastatic colorectal cancer without active liver metastases, the AI-identified subgroup showed a 64% response rate compared to 9% in the remaining patients. The AI-identified group also demonstrated</description>
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