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   <title>Teva submits NDA for ecopipam to treat pediatric Tourette syndrome</title>
   <link>http://www.streetinsider.com/Corporate+News/Teva+submits+NDA+for+ecopipam+to+treat+pediatric+Tourette+syndrome/26666962.html</link>
   <description>&lt;p&gt;Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) submitted a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, an investigational treatment for pediatric Tourette syndrome, the company announced June 18, 2026.&lt;/p&gt;&lt;p&gt;Ecopipam is a selective dopamine D1 receptor antagonist and has received FDA Orphan Drug and Fast Track designations for the treatment of pediatric patients with Tourette syndrome. Orphan Drug designation applies to conditions affecting populations of 200,000 or fewer.&lt;/p&gt;&lt;p&gt;The NDA is supported by Phase 3 data published in &lt;em&gt;JAMA Neurology&lt;/em&gt;, which showed ecopipam significantly delayed time to relapse compared with placebo in pediatric patients</description>
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   <pubDate>Thu, 18 Jun 2026 16:58:01 -0400</pubDate>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Press+Releases/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
   <link>http://www.streetinsider.com/Globe+Newswire/Teva+Submits+NDA+for+Ecopipam%2C+a+First-in-Class+Investigational+Therapy+for+Pediatric+Tourette+Syndrome/26666954.html</link>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <title>Teva Submits NDA for Ecopipam, a First-in-Class Investigational Therapy for Pediatric Tourette Syndrome</title>
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&lt;ul type=&quot;disc&quot;&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;NDA submission supported by positive Phase 3 data recently published in JAMA Neurology.&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam is a first-in-class selective dopamine D1 receptor antagonist with a novel mechanism of action and has received FDA Orphan Drug and Fast Track designations&lt;/li&gt;&lt;li style=&quot;margin-bottom:8pt;&quot;&gt;Ecopipam could be the first FDA-approved treatment option for pediatric Tourette syndrome in more than a decade, if approved.&lt;br/&gt;&lt;/li&gt;&lt;/ul&gt;  &lt;p&gt;TEL AVIV, Israel, June  18, 2026  (GLOBE NEWSWIRE) -- Teva Pharmaceutical Industries Ltd. (NYSE and TASE: TEVA) today announced the submission of a New Drug Application (NDA) to the U.S. Food and Drug Administration (FDA) for ecopipam, a</description>
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   <pubDate>Thu, 18 Jun 2026 16:15:00 -0400</pubDate>
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   <title>Form  4          Immuneering Corp          For: Jun 15  Filed by: Hall Brett Matthew</title>
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   <pubDate>Tue, 16 Jun 2026 16:15:00 -0400</pubDate>
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   <title>Form  4          Immuneering Corp          For: Jun 15  Filed by: Hall Brett Matthew</title>
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   <title>Form  4          Immuneering Corp          For: Jun 15  Filed by: Hall Brett Matthew</title>
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   <title>Form  4          Immuneering Corp          For: Jun 15  Filed by: Hall Brett Matthew</title>
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   <title>Form  4          TEVA PHARMACEUTICAL INDU  For: Jun 11  Filed by: Kalif Eliyahu Sharon</title>
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   <pubDate>Tue, 16 Jun 2026 08:28:00 -0400</pubDate>
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   <title>Form  4          TEVA PHARMACEUTICAL INDU  For: Jun 11  Filed by: Kalif Eliyahu Sharon</title>
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   <pubDate>Tue, 16 Jun 2026 08:28:00 -0400</pubDate>
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   <title>Form  4          TEVA PHARMACEUTICAL INDU  For: Jun 11  Filed by: Kalif Eliyahu Sharon</title>
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   <title>Form  8-K        Immuneering Corp          For: Jun 11</title>
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   <pubDate>Mon, 15 Jun 2026 16:12:00 -0400</pubDate>
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   <title>Form  8-K        Immuneering Corp          For: Jun 11</title>
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   <title>Form  8-K        Immuneering Corp          For: Jun 11</title>
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