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   <title>Form  4          Armata Pharmaceuticals,   For: Jul 10  Filed by: Birx Deborah</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+10++Filed+by%3A+Birx+Deborah/26768510.html</link>
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   <pubDate>Tue, 14 Jul 2026 16:19:00 -0400</pubDate>
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   <title>Form  4          Armata Pharmaceuticals,   For: Jul 10  Filed by: Birx Deborah</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+10++Filed+by%3A+Birx+Deborah/26768510.html</link>
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   <pubDate>Tue, 14 Jul 2026 16:19:00 -0400</pubDate>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 13</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+13/26759669.html</link>
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   <pubDate>Mon, 13 Jul 2026 07:11:00 -0400</pubDate>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 13</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+13/26759669.html</link>
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   <pubDate>Mon, 13 Jul 2026 07:11:00 -0400</pubDate>
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   <title>FDA agrees to Armata's pediatric study plan for AP-SA02 bacteremia drug</title>
   <link>http://www.streetinsider.com/Corporate+News/FDA+agrees+to+Armata%27s+pediatric+study+plan+for+AP-SA02+bacteremia+drug/26759567.html</link>
   <description>&lt;p&gt;Armata Pharmaceuticals, Inc. (NYSE American: ARMP) announced it has received agreement from the U.S. Food and Drug Administration on an Agreed Initial Pediatric Study Plan for AP-SA02, its bacteriophage therapeutic candidate for the adjunct treatment of complicated &lt;em&gt;Staphylococcus aureus&lt;/em&gt; bacteremia.&lt;/p&gt;&lt;p&gt;The agreement establishes a regulatory framework for evaluating AP-SA02 in pediatric patients up to 17 years of age. Under the Pediatric Research Equity Act, the FDA agreed that pediatric studies should be deferred until adult safety and efficacy data are generated, given that disease pathophysiology and treatment response in &lt;em&gt;S. aureus&lt;/em&gt; bacteremia are consistent across age groups.&lt;/p&gt;&lt;p&gt;Following completion of the adult</description>
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   <pubDate>Mon, 13 Jul 2026 07:00:52 -0400</pubDate>
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   <title>FDA agrees to Armata's pediatric study plan for AP-SA02 bacteremia drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+agrees+to+Armata%27s+pediatric+study+plan+for+AP-SA02+bacteremia+drug/26759567.html</link>
   <description>&lt;p&gt;Armata Pharmaceuticals, Inc. (NYSE American: ARMP) announced it has received agreement from the U.S. Food and Drug Administration on an Agreed Initial Pediatric Study Plan for AP-SA02, its bacteriophage therapeutic candidate for the adjunct treatment of complicated &lt;em&gt;Staphylococcus aureus&lt;/em&gt; bacteremia.&lt;/p&gt;&lt;p&gt;The agreement establishes a regulatory framework for evaluating AP-SA02 in pediatric patients up to 17 years of age. Under the Pediatric Research Equity Act, the FDA agreed that pediatric studies should be deferred until adult safety and efficacy data are generated, given that disease pathophysiology and treatment response in &lt;em&gt;S. aureus&lt;/em&gt; bacteremia are consistent across age groups.&lt;/p&gt;&lt;p&gt;Following completion of the adult</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/PRNewswire/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/PRNewswire/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/PRNewswire/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Armata Pharmaceuticals Receives Agreement from FDA on Initial Pediatric Study Plan for AP-SA02 for the Treatment of Complicated Staphylococcus aureus Bacteremia</title>
   <link>http://www.streetinsider.com/PRNewswire/Armata+Pharmaceuticals+Receives+Agreement+from+FDA+on+Initial+Pediatric+Study+Plan+for+AP-SA02+for+the+Treatment+of+Complicated+Staphylococcus+aureus+Bacteremia/26759524.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Fulfills important regulatory milestone for AP-SA02 on the path toward a future BLA and supports expansion into pediatric patients&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.losang&quot; idsrc=&quot;xmltag.org&quot; &gt;LOS ANGELES&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 13, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;AMEX:ARMP&quot; idsrc=&quot;xmltag.org&quot; &gt;Armata Pharmaceuticals, Inc.&lt;/span&gt; (NYSE American: ARMP) (&quot;Armata&quot; or the &quot;Company&quot;), a late clinical-stage biotechnology company focused on the development of high-purity, pathogen-specific bacteriophage therapeutics for the treatment of antibiotic-resistant and difficult-to-treat bacterial infections, today announced that it has received agreement from the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (the &quot;FDA&quot;) on an Agreed Initial Pediatric Study Plan (&quot;Agreed iPSP&quot;), which establishes the agreed</description>
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   <title>Form  S-8        Armata Pharmaceuticals,              </title>
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   <pubDate>Mon, 13 Jul 2026 06:02:00 -0400</pubDate>
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   <title>Form  S-8        Armata Pharmaceuticals,              </title>
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   <pubDate>Mon, 13 Jul 2026 06:02:00 -0400</pubDate>
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   <title>Form  8-K/A      Armata Pharmaceuticals,   For: Apr 24</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-KA++++++Armata+Pharmaceuticals%2C+++For%3A+Apr+24/26685794.html</link>
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   <pubDate>Wed, 24 Jun 2026 16:19:00 -0400</pubDate>
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   <title>Form  8-K/A      Armata Pharmaceuticals,   For: Apr 24</title>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jun 23</title>
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   <pubDate>Tue, 23 Jun 2026 07:11:00 -0400</pubDate>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jun 23</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jun+23/26675761.html</link>
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   <pubDate>Tue, 23 Jun 2026 07:11:00 -0400</pubDate>
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   <title>Armata gets $2.5M more in DoD funding for bacteriophage drug</title>
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   <description>&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) announced it has received an additional $2.5 million in non-dilutive funding from the U.S. Department of Defense (DoD) to support the development of its lead clinical candidate AP-SA02, a bacteriophage therapeutic targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia.&lt;/p&gt;&lt;p&gt;The funding was received through the Medical Technology Enterprise Consortium and is managed by the Naval Medical Research Command with contributions from the Defense Health Agency and Joint Warfighter Medical Research Program. Total non-dilutive DoD funding for the program now stands at $28.7 million.&lt;/p&gt;&lt;p&gt;The additional $2.5 million is designated to fund activities supporting Phase 3 readiness of AP-SA02, which Armata plans</description>
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   <pubDate>Tue, 23 Jun 2026 07:01:23 -0400</pubDate>
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