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   <title>XORTX Therapeutics Inc (XRTX) Provides Update on FDA Type B Meeting Request</title>
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   <description>&lt;p&gt;XORTX Therapeutics Inc. (&quot;&lt;strong&gt;XORTX&lt;/strong&gt;&quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment of gout. The Type B meeting conducted by the FDA, included review of chemistry, manufacturing, pharmacology, toxicology and clinical evidence to support the Company’s XRx-026 program for the treatment</description>
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   <title>XORTX Therapeutics Inc (XRTX) Provides Update on FDA Type B Meeting Request</title>
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   <description>&lt;p&gt;XORTX Therapeutics Inc. (&quot;&lt;strong&gt;XORTX&lt;/strong&gt;&quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment of gout. The Type B meeting conducted by the FDA, included review of chemistry, manufacturing, pharmacology, toxicology and clinical evidence to support the Company’s XRx-026 program for the treatment</description>
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   <title>XORTX Therapeutics Inc (XRTX) Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/FDA/XORTX+Therapeutics+Inc+%28XRTX%29+Provides+Update+on+FDA+Type+B+Meeting+Request/24712135.html</link>
   <description>&lt;p&gt;XORTX Therapeutics Inc. (&quot;&lt;strong&gt;XORTX&lt;/strong&gt;&quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment of gout. The Type B meeting conducted by the FDA, included review of chemistry, manufacturing, pharmacology, toxicology and clinical evidence to support the Company’s XRx-026 program for the treatment</description>
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   <title>XORTX Therapeutics Inc (XRTX) Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/FDA/XORTX+Therapeutics+Inc+%28XRTX%29+Provides+Update+on+FDA+Type+B+Meeting+Request/24712135.html</link>
   <description>&lt;p&gt;XORTX Therapeutics Inc. (&quot;&lt;strong&gt;XORTX&lt;/strong&gt;&quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment of gout. The Type B meeting conducted by the FDA, included review of chemistry, manufacturing, pharmacology, toxicology and clinical evidence to support the Company’s XRx-026 program for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Press+Releases/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Press+Releases/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Press+Releases/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Press+Releases/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Press+Releases/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Provides Update on FDA Type B Meeting Request</title>
   <link>http://www.streetinsider.com/Globe+Newswire/XORTX+Provides+Update+on+FDA+Type+B+Meeting+Request/24712005.html</link>
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&lt;p align=&quot;center&quot;&gt;● &lt;strong&gt;XORTX will focus on key steps &lt;/strong&gt;&lt;br/&gt;&lt;strong&gt;to advance a NDA filing for Gout indication &lt;/strong&gt;●&lt;/p&gt;  &lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  30, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease, is pleased to announce it has received responses from the US Food and Drug Administration (the “FDA”) and clarified key steps for a new drug application (“NDA”) for the Company’s novel proprietary formulation of oxypurinol for the treatment</description>
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   <title>XORTX Announces Grant of European Patent</title>
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&lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  28, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease , is pleased to announce receipt of notification that the patent “Xanthine Oxidase Inhibitor Formulations” will be granted by the European Patent Office. The patent covers compositions and methods of formulating using XORTX’s proprietary formulations of xanthine oxidase inhibitors (“XOI”) for the treatment of health consequences of chronically high uric acid, gout, renal, cardiovascular and other</description>
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   <title>XORTX Announces Grant of European Patent</title>
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&lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  28, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease , is pleased to announce receipt of notification that the patent “Xanthine Oxidase Inhibitor Formulations” will be granted by the European Patent Office. The patent covers compositions and methods of formulating using XORTX’s proprietary formulations of xanthine oxidase inhibitors (“XOI”) for the treatment of health consequences of chronically high uric acid, gout, renal, cardiovascular and other</description>
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   <title>XORTX Announces Grant of European Patent</title>
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&lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  28, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease , is pleased to announce receipt of notification that the patent “Xanthine Oxidase Inhibitor Formulations” will be granted by the European Patent Office. The patent covers compositions and methods of formulating using XORTX’s proprietary formulations of xanthine oxidase inhibitors (“XOI”) for the treatment of health consequences of chronically high uric acid, gout, renal, cardiovascular and other</description>
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&lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  28, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease , is pleased to announce receipt of notification that the patent “Xanthine Oxidase Inhibitor Formulations” will be granted by the European Patent Office. The patent covers compositions and methods of formulating using XORTX’s proprietary formulations of xanthine oxidase inhibitors (“XOI”) for the treatment of health consequences of chronically high uric acid, gout, renal, cardiovascular and other</description>
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&lt;p align=&quot;justify&quot;&gt;CALGARY, Alberta, April  28, 2025  (GLOBE NEWSWIRE) -- XORTX Therapeutics Inc. (&amp;quot;&lt;strong&gt;XORTX&lt;/strong&gt;&amp;quot; or the “&lt;strong&gt;Company&lt;/strong&gt;”) (NASDAQ: XRTX | TSXV: XRTX | Frankfurt: ANU), a late stage clinical pharmaceutical company focused on developing innovative therapies to treat gout and progressive kidney disease , is pleased to announce receipt of notification that the patent “Xanthine Oxidase Inhibitor Formulations” will be granted by the European Patent Office. The patent covers compositions and methods of formulating using XORTX’s proprietary formulations of xanthine oxidase inhibitors (“XOI”) for the treatment of health consequences of chronically high uric acid, gout, renal, cardiovascular and other</description>
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