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   <title>Form  6-K        Clearmind Medicine Inc.   For: Jun 01</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+Jun+01/26583516.html</link>
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   <pubDate>Mon, 01 Jun 2026 16:07:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CMND</category>
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   <title>Form  6-K        Clearmind Medicine Inc.   For: Jun 01</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+Jun+01/26583516.html</link>
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   <pubDate>Mon, 01 Jun 2026 16:07:00 -0400</pubDate>
      	<category domain="http://rss.financialcontent.com/stocksymbol">CMND</category>
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   <title>Clearmind Medicine files Japanese patent for depression treatment compound</title>
   <link>http://www.streetinsider.com/Corporate+News/Clearmind+Medicine+files+Japanese+patent+for+depression+treatment+compound/26571150.html</link>
   <description>&lt;p&gt;Clearmind Medicine Inc. (NASDAQ: CMND) announced the publication of a Japanese patent application for its proprietary compositions containing 5-Methoxy-2-aminoindan (MEAI) for depression treatment, according to a company statement.&lt;/p&gt;&lt;p&gt;The Vancouver-based clinical-stage biotech company describes MEAI as a non-hallucinogenic molecule designed as an alternative to traditional antidepressants and psychedelic-based therapies. The filing adds to Clearmind's intellectual property portfolio, which includes 19 patent families and 31 granted patents.&lt;/p&gt;&lt;p&gt;Japan has approximately 3 million diagnosed cases of major depressive disorder, the company stated. The global anxiety and depression treatment market is estimated at $16-22.65 billion in 2025, with projections reaching $19-30 billion by 2030-2031.&lt;/p&gt;&lt;p&gt;Clearmind is</description>
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   <pubDate>Fri, 29 May 2026 08:41:16 -0400</pubDate>
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   <title>Form  6-K        Clearmind Medicine Inc.   For: May 29</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+May+29/26571125.html</link>
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   <pubDate>Fri, 29 May 2026 08:35:00 -0400</pubDate>
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   <title>Form  6-K        Clearmind Medicine Inc.   For: May 29</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+May+29/26571125.html</link>
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   <pubDate>Fri, 29 May 2026 08:35:00 -0400</pubDate>
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   <title>Clearmind Medicine Advances Global Intellectual Property Portfolio with Japanese Patent Filing for Innovative Psychedelic- Based Depression Treatment</title>
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   <description>&lt;p&gt;Vancouver, Canada, May  29, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &quot;Company&quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced the publication of a Japanese Patent Application for its proprietary compositions comprising 5-Methoxy-2-aminoindan (MEAI) for the treatment of depression.&lt;/p&gt;  &lt;p&gt;This advancement  strengthens Clearmind’s robust intellectual property portfolio, which already includes multiple granted patents and applications worldwide. MEAI, the company’s flagship non-hallucinogenic molecule, is designed to offer a safer, more accessible alternative to traditional antidepressants and</description>
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   <pubDate>Fri, 29 May 2026 08:32:00 -0400</pubDate>
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   <title>Clearmind Medicine Advances Global Intellectual Property Portfolio with Japanese Patent Filing for Innovative Psychedelic- Based Depression Treatment</title>
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   <description>&lt;p&gt;Vancouver, Canada, May  29, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &quot;Company&quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced the publication of a Japanese Patent Application for its proprietary compositions comprising 5-Methoxy-2-aminoindan (MEAI) for the treatment of depression.&lt;/p&gt;  &lt;p&gt;This advancement  strengthens Clearmind’s robust intellectual property portfolio, which already includes multiple granted patents and applications worldwide. MEAI, the company’s flagship non-hallucinogenic molecule, is designed to offer a safer, more accessible alternative to traditional antidepressants and</description>
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   <pubDate>Fri, 29 May 2026 08:32:00 -0400</pubDate>
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   <title>Form  6-K        Clearmind Medicine Inc.   For: May 26</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+May+26/26546479.html</link>
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   <pubDate>Tue, 26 May 2026 08:30:00 -0400</pubDate>
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   <title>Form  6-K        Clearmind Medicine Inc.   For: May 26</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++6-K++++++++Clearmind+Medicine+Inc.+++For%3A+May+26/26546479.html</link>
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   <pubDate>Tue, 26 May 2026 08:30:00 -0400</pubDate>
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   <title>Clearmind Medicine receives Johns Hopkins approval for CMND-100 trial parts</title>
   <link>http://www.streetinsider.com/Corporate+News/Clearmind+Medicine+receives+Johns+Hopkins+approval+for+CMND-100+trial+parts/26546393.html</link>
   <description>&lt;p&gt;Clearmind Medicine Inc. (NASDAQ: CMND) received approval from the Johns Hopkins Medicine Institutional Review Board to advance its Phase I/II clinical trial of CMND-100 to Parts B and C, the company announced May 26.&lt;/p&gt;&lt;p&gt;The multicenter study examines single and multiple dose tolerability, safety and pharmacokinetics of CMND-100 in healthy volunteers and subjects with alcohol use disorder. The approval permits the company to proceed with the next phases of the trial following completion of earlier stages.&lt;/p&gt;&lt;p&gt;CMND-100 is described as a non-hallucinogenic compound based on MEAI being developed as a treatment for alcohol use disorder. The drug candidate is part of what</description>
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   <pubDate>Tue, 26 May 2026 08:25:29 -0400</pubDate>
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   <title>Clearmind Medicine receives Johns Hopkins approval for CMND-100 trial parts</title>
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   <description>&lt;p&gt;Clearmind Medicine Inc. (NASDAQ: CMND) received approval from the Johns Hopkins Medicine Institutional Review Board to advance its Phase I/II clinical trial of CMND-100 to Parts B and C, the company announced May 26.&lt;/p&gt;&lt;p&gt;The multicenter study examines single and multiple dose tolerability, safety and pharmacokinetics of CMND-100 in healthy volunteers and subjects with alcohol use disorder. The approval permits the company to proceed with the next phases of the trial following completion of earlier stages.&lt;/p&gt;&lt;p&gt;CMND-100 is described as a non-hallucinogenic compound based on MEAI being developed as a treatment for alcohol use disorder. The drug candidate is part of what</description>
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   <pubDate>Tue, 26 May 2026 08:25:29 -0400</pubDate>
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   <title>Clearmind Medicine Announces Johns Hopkins IRB Approval to Advance CMND-100 Phase I/II Clinical Trial to the Next Parts</title>
   <link>http://www.streetinsider.com/Press+Releases/Clearmind+Medicine+Announces+Johns+Hopkins+IRB+Approval+to+Advance+CMND-100+Phase+III+Clinical+Trial+to+the+Next+Parts/26546389.html</link>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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   <title>Clearmind Medicine Announces Johns Hopkins IRB Approval to Advance CMND-100 Phase I/II Clinical Trial to the Next Parts</title>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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   <title>Clearmind Medicine Announces Johns Hopkins IRB Approval to Advance CMND-100 Phase I/II Clinical Trial to the Next Parts</title>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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&lt;p&gt;Vancouver, Canada, May  26, 2026  (GLOBE NEWSWIRE) --  Clearmind Medicine Inc. (Nasdaq: CMND) (“Clearmind” or the &amp;quot;Company&amp;quot;), a clinical-stage biotech company focused on the discovery and development of novel, non-hallucinogenic, second-generation, neuroplastogen-derived therapeutics to solve major under-treated health problems, today announced that the Johns Hopkins Medicine Institutional Review Board (JHM-IRB) has granted approval for its ongoing Phase I/II clinical trial of CMND-100.&lt;/p&gt;  &lt;p&gt;The approval advances the multicenter study titled “A Phase I/II Single and Multiple Dose Tolerability, Safety and Pharmacokinetic Study of CMND-100 in Healthy Volunteers and Alcohol Use Disorder (AUD) Subjects: Parts A, B, and</description>
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