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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 17</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+17/26786942.html</link>
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   <pubDate>Mon, 20 Jul 2026 07:13:00 -0400</pubDate>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 17</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+17/26786942.html</link>
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   <pubDate>Mon, 20 Jul 2026 07:13:00 -0400</pubDate>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 20</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+20/26786948.html</link>
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   <title>Form  8-K        Armata Pharmaceuticals,   For: Jul 20</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++8-K++++++++Armata+Pharmaceuticals%2C+++For%3A+Jul+20/26786948.html</link>
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   <pubDate>Mon, 20 Jul 2026 07:13:00 -0400</pubDate>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
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&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata submits Phase 3 protocol to FDA for bacteriophage drug AP-SA02</title>
   <link>http://www.streetinsider.com/FDA/Armata+submits+Phase+3+protocol+to+FDA+for+bacteriophage+drug+AP-SA02/26786839.html</link>
   <description>

&lt;p&gt;Armata Pharmaceuticals (NYSE American: ARMP) has submitted its complete Phase 3 superiority protocol to the U.S. Food and Drug Administration for AP-SA02, its bacteriophage product candidate targeting &lt;i&gt;Staphylococcus aureus&lt;/i&gt; bacteremia, according to a press release dated July 20, 2026.&lt;/p&gt;

&lt;p&gt;The company also submitted responses to all FDA comments on clinical, chemistry, manufacturing, and controls topics raised during the End-of-Phase 2 meeting. Armata said it has completed four engineering runs of AP-SA02 at its manufacturing facility in Los Angeles, with production of clinical trial material identified as the next planned step.&lt;/p&gt;

&lt;p&gt;The company said its Phase 3 study remains on track to begin</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Achieves+Key+Progress+Across+Clinical%2C+Regulatory+and+Manufacturing+Activities+Supporting+Planned+Phase+3+Initiation+of+AP-SA02/26786824.html</link>
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&lt;div class=&quot;xn-content&quot;&gt;
&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
   <link>http://www.streetinsider.com/Press+Releases/Armata+Pharmaceuticals+Achieves+Key+Progress+Across+Clinical%2C+Regulatory+and+Manufacturing+Activities+Supporting+Planned+Phase+3+Initiation+of+AP-SA02/26786824.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;FDA submissions address all feedback on clinical, CMC, and regulatory topics from the End-of-Phase 2 meeting&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Four AP-SA02 engineering runs completed; clinical trial material production is the next planned manufacturing step&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;Phase 3 superiority study remains on track to initiate 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.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 20, 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 significant clinical, regulatory, manufacturing</description>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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   <title>Armata Pharmaceuticals Achieves Key Progress Across Clinical, Regulatory and Manufacturing Activities Supporting Planned Phase 3 Initiation of AP-SA02</title>
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