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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>FDA clears Atrium Therapeutics IND for rare heart disease drug</title>
   <link>http://www.streetinsider.com/FDA/FDA+clears+Atrium+Therapeutics+IND+for+rare+heart+disease+drug/26764439.html</link>
   <description>

&lt;p&gt;Atrium Therapeutics, Inc. (Nasdaq: RNA) announced that the U.S. Food and Drug Administration has cleared its Investigational New Drug application for ATR 1072, allowing the company to proceed with a Phase 1/2 clinical trial for the treatment of PRKAG2 syndrome, a rare genetic cardiomyopathy.&lt;/p&gt;

&lt;p&gt;The trial, called Corventis, is an open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, and efficacy of ATR 1072. It will enroll approximately 37 participants across two parts: Part A will consist of multiple ascending dose cohorts to assess safety and inform dose selection, and Part B will be a single-arm expansion cohort at</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+FDA+Clearance+of+Investigational+New+Drug+Application+for+ATR+1072+for+Treatment+of+PRKAG2+Syndrome/26764431.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+FDA+Clearance+of+Investigational+New+Drug+Application+for+ATR+1072+for+Treatment+of+PRKAG2+Syndrome/26764431.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+FDA+Clearance+of+Investigational+New+Drug+Application+for+ATR+1072+for+Treatment+of+PRKAG2+Syndrome/26764431.html</link>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces FDA Clearance of Investigational New Drug Application for ATR 1072 for Treatment of PRKAG2 Syndrome</title>
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&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- ATR 1072 is the company's first precision cardiology program to enter the clinic --&lt;/i&gt;&lt;/p&gt;&lt;p class=&quot;prntac&quot;&gt;&lt;i&gt;-- &lt;span value=&quot;ACORN:3169166301&quot; idsrc=&quot;xmltag.org&quot; &gt;Corventis&lt;/span&gt;&lt;/i&gt;™ &lt;i&gt;will be the first clinical trial for people living with PRKAG2 syndrome that evaluates a potential treatment for the underlying cause of the disease --&lt;/i&gt;&lt;/p&gt;&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;July 14, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;), a biopharmaceutical company dedicated to delivering RNA therapeutics to the heart, announced today that the &lt;span value=&quot;ACORN:0682203466&quot; idsrc=&quot;xmltag.org&quot; &gt;U.S. Food and Drug Administration&lt;/span&gt; (FDA) has cleared its Investigational New Drug (IND) application</description>
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   <title>Atrium Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+Inducement+Grants+under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26679440.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 23, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;) today announced it awarded inducement grants on &lt;chron&gt;June 20, 2026&lt;/chron&gt; under the Company's 2026 Employment Inducement Incentive Award Plan (the &quot;2026 Inducement Plan&quot;) as a material inducement to the employment of eight non-executive individuals newly hired by the Company.&lt;/p&gt;
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   <pubDate>Tue, 23 Jun 2026 16:05:00 -0400</pubDate>
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   <title>Atrium Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+Inducement+Grants+under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26679440.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 23, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;) today announced it awarded inducement grants on &lt;chron&gt;June 20, 2026&lt;/chron&gt; under the Company's 2026 Employment Inducement Incentive Award Plan (the &quot;2026 Inducement Plan&quot;) as a material inducement to the employment of eight non-executive individuals newly hired by the Company.&lt;/p&gt;
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   <pubDate>Tue, 23 Jun 2026 16:05:00 -0400</pubDate>
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   <title>Atrium Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+Inducement+Grants+under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26679440.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 23, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;) today announced it awarded inducement grants on &lt;chron&gt;June 20, 2026&lt;/chron&gt; under the Company's 2026 Employment Inducement Incentive Award Plan (the &quot;2026 Inducement Plan&quot;) as a material inducement to the employment of eight non-executive individuals newly hired by the Company.&lt;/p&gt;
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   <title>Atrium Therapeutics Announces Inducement Grants under Nasdaq Listing Rule 5635(c)(4)</title>
   <link>http://www.streetinsider.com/Press+Releases/Atrium+Therapeutics+Announces+Inducement+Grants+under+Nasdaq+Listing+Rule+5635%28c%29%284%29/26679440.html</link>
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&lt;p&gt;&lt;span class=&quot;legendSpanClass&quot;&gt;&lt;location value=&quot;LU/us.ca.sandgo&quot; idsrc=&quot;xmltag.org&quot; &gt;SAN DIEGO&lt;/location&gt;&lt;/span&gt;, &lt;span class=&quot;legendSpanClass&quot;&gt;&lt;chron&gt;June 23, 2026&lt;/chron&gt;&lt;/span&gt; /PRNewswire/ -- &lt;span value=&quot;ACORN:5021700326&quot; idsrc=&quot;xmltag.org&quot; &gt;Atrium Therapeutics, Inc.&lt;/span&gt; (Nasdaq: RNA) (the &quot;Company&quot;) today announced it awarded inducement grants on &lt;chron&gt;June 20, 2026&lt;/chron&gt; under the Company's 2026 Employment Inducement Incentive Award Plan (the &quot;2026 Inducement Plan&quot;) as a material inducement to the employment of eight non-executive individuals newly hired by the Company.&lt;/p&gt;
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