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   <title>Form  4          Cingulate Inc.            For: Feb 13  Filed by: Hargroves Thomas Jeffrey</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Cingulate+Inc.++++++++++++For%3A+Feb+13++Filed+by%3A+Hargroves+Thomas+Jeffrey/26618726.html</link>
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   <pubDate>Mon, 08 Jun 2026 19:02:00 -0400</pubDate>
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   <title>Form  4          Cingulate Inc.            For: Feb 13  Filed by: Hargroves Thomas Jeffrey</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++4++++++++++Cingulate+Inc.++++++++++++For%3A+Feb+13++Filed+by%3A+Hargroves+Thomas+Jeffrey/26618726.html</link>
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   <pubDate>Mon, 08 Jun 2026 19:02:00 -0400</pubDate>
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   <title>Form  3          Cingulate Inc.            For: Feb 13  Filed by: Hargroves Thomas Jeffrey</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++3++++++++++Cingulate+Inc.++++++++++++For%3A+Feb+13++Filed+by%3A+Hargroves+Thomas+Jeffrey/26618717.html</link>
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   <pubDate>Mon, 08 Jun 2026 19:00:00 -0400</pubDate>
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   <title>Form  3          Cingulate Inc.            For: Feb 13  Filed by: Hargroves Thomas Jeffrey</title>
   <link>http://www.streetinsider.com/SEC+Filings/Form++3++++++++++Cingulate+Inc.++++++++++++For%3A+Feb+13++Filed+by%3A+Hargroves+Thomas+Jeffrey/26618717.html</link>
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   <pubDate>Mon, 08 Jun 2026 19:00:00 -0400</pubDate>
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   <title>Stonegate Capital Partners Updates Coverage on Cingulate Inc. (CING) 1Q26</title>
   <link>http://www.streetinsider.com/Press+Releases/Stonegate+Capital+Partners+Updates+Coverage+on+Cingulate+Inc.+%28CING%29+1Q26/26606487.html</link>
   <description>&lt;p&gt;      Dallas, Texas--(Newsfile Corp. - June 4, 2026) - Cingulate Inc. (NASDAQ: CING): Stonegate Capital Partners updates coverage on Cingulate Inc. (NASDAQ: CING). Cingulate's latest update shifts the near-term      CTx-1301 setup from a PDUFA driven approval event to a CMC-driven resubmission process, while leaving the core product thesis intact based on the information disclosed. The FDA issued a      Complete Response Letter for the CTx-1301 NDA focused on specific CMC information requests, with no current clinical safety or efficacy concerns identified. In our view, the key</description>
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   <pubDate>Thu, 04 Jun 2026 16:48:00 -0400</pubDate>
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   <title>Stonegate Capital Partners Updates Coverage on Cingulate Inc. (CING) 1Q26</title>
   <link>http://www.streetinsider.com/Newsfile/Stonegate+Capital+Partners+Updates+Coverage+on+Cingulate+Inc.+%28CING%29+1Q26/26606487.html</link>
   <description>&lt;p&gt;      Dallas, Texas--(Newsfile Corp. - June 4, 2026) - Cingulate Inc. (NASDAQ: CING): Stonegate Capital Partners updates coverage on Cingulate Inc. (NASDAQ: CING). Cingulate's latest update shifts the near-term      CTx-1301 setup from a PDUFA driven approval event to a CMC-driven resubmission process, while leaving the core product thesis intact based on the information disclosed. The FDA issued a      Complete Response Letter for the CTx-1301 NDA focused on specific CMC information requests, with no current clinical safety or efficacy concerns identified. In our view, the key</description>
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   <pubDate>Thu, 04 Jun 2026 16:48:00 -0400</pubDate>
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   <title>Form  8-K        Cingulate Inc.            For: Jun 02</title>
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   <pubDate>Tue, 02 Jun 2026 08:10:00 -0400</pubDate>
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   <title>Form  8-K        Cingulate Inc.            For: Jun 02</title>
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   <pubDate>Tue, 02 Jun 2026 08:10:00 -0400</pubDate>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Corporate+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <pubDate>Tue, 02 Jun 2026 08:01:09 -0400</pubDate>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Corporate+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/FDA/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/FDA/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Hot+Corp.+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>FDA issues complete response letter for Cingulate's ADHD drug CTx-1301</title>
   <link>http://www.streetinsider.com/Hot+FDA+News/FDA+issues+complete+response+letter+for+Cingulate%27s+ADHD+drug+CTx-1301/26587805.html</link>
   <description>&lt;p&gt;Cingulate Inc. (NASDAQ: CING) received a Complete Response Letter from the U.S. Food and Drug Administration for its New Drug Application for CTx-1301, a treatment for Attention Deficit/Hyperactivity Disorder, according to a company statement.&lt;/p&gt;&lt;p&gt;The FDA response identified specific Chemistry, Manufacturing and Controls information requests and did not raise concerns regarding the clinical safety or efficacy of CTx-1301, the company said. CTx-1301 is a once-daily tablet containing dexmethylphenidate HCl that uses Cingulate's Precision Timed Release platform to deliver three timed releases of medication throughout the day.&lt;/p&gt;&lt;p&gt;&quot;We are encouraged that the FDA's response was limited to specific information requests related to CMC</description>
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   <title>Cingulate Receives Complete Response Letter from FDA for CTx-1301</title>
   <link>http://www.streetinsider.com/Press+Releases/Cingulate+Receives+Complete+Response+Letter+from+FDA+for+CTx-1301/26587673.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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   <title>Cingulate Receives Complete Response Letter from FDA for CTx-1301</title>
   <link>http://www.streetinsider.com/Press+Releases/Cingulate+Receives+Complete+Response+Letter+from+FDA+for+CTx-1301/26587673.html</link>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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   <title>Cingulate Receives Complete Response Letter from FDA for CTx-1301</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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   <title>Cingulate Receives Complete Response Letter from FDA for CTx-1301</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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   <title>Cingulate Receives Complete Response Letter from FDA for CTx-1301</title>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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&lt;p align=&quot;center&quot;&gt;&lt;em&gt;No Clinical Safety or Efficacy Concerns Currently Identified &lt;/em&gt;&lt;br/&gt;&lt;em&gt;Agency Feedback Primarily Focused on CMC-Related Requests&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company Plans Prompt Response and Submission of Requested Information&lt;/em&gt;&lt;br/&gt;&lt;em&gt;Company is Well Capitalized with Nearly $30 Million Cash on Hand&lt;/em&gt;&lt;/p&gt;  &lt;p align=&quot;left&quot;&gt;KANSAS CITY, Kan., June  02, 2026  (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform to develop a pipeline of next-generation products, today announced that the U.S. Food and Drug Administration (“FDA”) has issued a Complete Response Letter for its New Drug Application (“NDA”) for CTx-1301 (dexmethylphenidate HCl) for the treatment of</description>
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