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   <title>Bioxytran reports positive results from COVID-19 antiviral trial</title>
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&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a Phase 1b/2a clinical study of its oral antiviral drug ProLectin-M in hospitalized patients with mild to moderate COVID-19. The randomized, double-blind, placebo-controlled study enrolled 39 participants in India.&lt;/p&gt;

&lt;p&gt;The study showed that patients receiving the highest dose of ProLectin-M at 16,800 mg per day achieved statistically significant earlier viral clearance compared to placebo. By Day 5, 90% of participants in the highest-dose group achieved non-detectable viral shedding, compared to 20% in the placebo group. The difference was statistically significant with a p-value of 0.001.&lt;/p&gt;

&lt;p&gt;Clinical improvement also occurred faster in the highest-dose group, with</description>
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   <pubDate>Mon, 02 Mar 2026 11:40:11 +0000</pubDate>
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   <title>Bioxytran, Inc. Reports Positive Phase 1b/2a Clinical Study Results for ProLectin-M, a Broad-Range Antiviral Drug in Mild to Moderate COVID-19 </title>
   <link>http://www.streetinsider.com/Press+Releases/Bioxytran%2C+Inc.+Reports+Positive+Phase+1b2a+Clinical+Study+Results+for+ProLectin-M%2C+a+Broad-Range+Antiviral+Drug+in+Mild+to+Moderate+COVID-19+/26089582.html</link>
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      &lt;p&gt;&lt;strong id=&quot;dateline&quot;&gt;BOSTON, MA / &lt;a href='https://www.accessnewswire.com/'&gt;ACCESS Newswire&lt;/a&gt; / March 2, 2026 / &lt;/strong&gt;Bioxytran, Inc. (OTCQB:BIXT), a clinical-stage biotechnology company developing carbohydrate-based therapeutics, today announced results from a randomized, double-blind, placebo-controlled Phase 1b/2a clinical study evaluating oral ProLectin-M in hospitalized patients with mild to moderate COVID-19 caused by SARS-CoV-2.&lt;/p&gt;&lt;p&gt;The study showed that the highest evaluated dose of ProLectin-M (16,800 mg/day) was associated with statistically significant earlier viral clearance and faster clinical improvement by Day 5 compared with placebo, while demonstrating a favorable safety and tolerability profile. By Day 7, viral clearance was observed across all</description>
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   <title>Bioxytran, Inc. Reports Positive Phase 1b/2a Clinical Study Results for ProLectin-M, a Broad-Range Antiviral Drug in Mild to Moderate COVID-19 </title>
   <link>http://www.streetinsider.com/ACCESS+Newswire/Bioxytran%2C+Inc.+Reports+Positive+Phase+1b2a+Clinical+Study+Results+for+ProLectin-M%2C+a+Broad-Range+Antiviral+Drug+in+Mild+to+Moderate+COVID-19+/26089582.html</link>
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      &lt;p&gt;&lt;strong id=&quot;dateline&quot;&gt;BOSTON, MA / &lt;a href='https://www.accessnewswire.com/'&gt;ACCESS Newswire&lt;/a&gt; / March 2, 2026 / &lt;/strong&gt;Bioxytran, Inc. (OTCQB:BIXT), a clinical-stage biotechnology company developing carbohydrate-based therapeutics, today announced results from a randomized, double-blind, placebo-controlled Phase 1b/2a clinical study evaluating oral ProLectin-M in hospitalized patients with mild to moderate COVID-19 caused by SARS-CoV-2.&lt;/p&gt;&lt;p&gt;The study showed that the highest evaluated dose of ProLectin-M (16,800 mg/day) was associated with statistically significant earlier viral clearance and faster clinical improvement by Day 5 compared with placebo, while demonstrating a favorable safety and tolerability profile. By Day 7, viral clearance was observed across all</description>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Mar 02</title>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Mar 02</title>
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   <title>Bioxytran Initiates Research Collaboration with University of Georgia to Evaluate Drug Candidate&amp;apos;s Ability to Block H5N1 Bird Flu Virus</title>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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   <title>Bioxytran Initiates Research Collaboration with University of Georgia to Evaluate Drug Candidate&amp;apos;s Ability to Block H5N1 Bird Flu Virus</title>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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   <title>Bioxytran Initiates Research Collaboration with University of Georgia to Evaluate Drug Candidate&amp;apos;s Ability to Block H5N1 Bird Flu Virus</title>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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&lt;p&gt;BOSTON, Massachusetts, Feb 23, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCQB: BIXT), a clinical-stage biotechnology company developing breakthrough antiviral treatments, today announced it has initiated a research collaboration with the University of Georgia (UGA) as part of a $100M grant to explore the efficacy of its lead drug candidate in blocking the Highly Pathogenic Avian Influenza (HPAI) H5N1 virus, commonly known as bird flu.&lt;/p&gt;&lt;p&gt;The collaboration follows a previously announced Non-Disclosure Agreement (NDA) signed in March 2025 and formalizes the framework for evaluating Bioxytran&amp;apos;s novel galectin antagonist as a potential therapeutic for infected poultry . The research is</description>
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   <title>Bioxytran, Inc. Announces Commercial Distribution Agreement with Khoury Medical LTD for A-SUQAR Dietary Supplement</title>
   <link>http://www.streetinsider.com/Press+Releases/Bioxytran%2C+Inc.+Announces+Commercial+Distribution+Agreement+with+Khoury+Medical+LTD+for+A-SUQAR+Dietary+Supplement/26008787.html</link>
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&lt;p&gt;BOSTON, Massachusetts, Feb 17, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCMKTS: BIXT) (&amp;quot;Bioxytran&amp;quot; or the &amp;quot;Company&amp;quot;), a biotechnology company developing galectin-targeting carbohydrate technologies with applications across infectious disease, metabolic health, and inflammation, today announced that it has entered into a commercial Distribution Agreement with Khoury Medical LTD (&amp;quot;Khoury Medical&amp;quot;), a company focused on the development and commercialization of plant-derived dietary supplements.&lt;/p&gt;&lt;p&gt;Under the agreement, Khoury Medical will commercialize A-SUQAR, a chewable dietary supplement containing Bioxytran&amp;apos;s proprietary partially hydrolyzed guar gum (PHGG) formulation, in permitted markets in accordance with the Distribution Agreement. The product is marketed as a dietary</description>
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   <pubDate>Tue, 17 Feb 2026 07:00:00 +0000</pubDate>
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   <title>Bioxytran, Inc. Announces Commercial Distribution Agreement with Khoury Medical LTD for A-SUQAR Dietary Supplement</title>
   <link>http://www.streetinsider.com/Press+Releases/Bioxytran%2C+Inc.+Announces+Commercial+Distribution+Agreement+with+Khoury+Medical+LTD+for+A-SUQAR+Dietary+Supplement/26008787.html</link>
   <description>
&lt;p&gt;BOSTON, Massachusetts, Feb 17, 2026 - (JCN Newswire) -  - Bioxytran, Inc. (OTCMKTS: BIXT) (&amp;quot;Bioxytran&amp;quot; or the &amp;quot;Company&amp;quot;), a biotechnology company developing galectin-targeting carbohydrate technologies with applications across infectious disease, metabolic health, and inflammation, today announced that it has entered into a commercial Distribution Agreement with Khoury Medical LTD (&amp;quot;Khoury Medical&amp;quot;), a company focused on the development and commercialization of plant-derived dietary supplements.&lt;/p&gt;&lt;p&gt;Under the agreement, Khoury Medical will commercialize A-SUQAR, a chewable dietary supplement containing Bioxytran&amp;apos;s proprietary partially hydrolyzed guar gum (PHGG) formulation, in permitted markets in accordance with the Distribution Agreement. The product is marketed as a dietary</description>
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   <pubDate>Tue, 17 Feb 2026 07:00:00 +0000</pubDate>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Feb 10</title>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Feb 10</title>
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   <title>Bioxytran reports viral clearance in phase 2 trial of ProLectin-M</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+viral+clearance+in+phase+2+trial+of+ProLectin-M/25979554.html</link>
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&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a Phase 2 trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo group participants.&lt;/p&gt;

&lt;p&gt;The randomized, double-blind, placebo-controlled trial enrolled 38 subjects with laboratory-confirmed acute viral infection. Participants received one of three ProLectin-M dose levels or placebo over seven days. All subjects completed the study.&lt;/p&gt;

&lt;p&gt;Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs. The company reported 100% of treated subjects achieved complete viral elimination by day 7, with statistical significance of p=.001 versus placebo. No viral rebounds occurred during a 14-day post-treatment observation period.&lt;/p&gt;

&lt;p&gt;According to</description>
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   <pubDate>Wed, 11 Feb 2026 07:47:59 +0000</pubDate>
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   <title>Bioxytran reports viral clearance in phase 2 trial of ProLectin-M</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+viral+clearance+in+phase+2+trial+of+ProLectin-M/25979554.html</link>
   <description>

&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a Phase 2 trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo group participants.&lt;/p&gt;

&lt;p&gt;The randomized, double-blind, placebo-controlled trial enrolled 38 subjects with laboratory-confirmed acute viral infection. Participants received one of three ProLectin-M dose levels or placebo over seven days. All subjects completed the study.&lt;/p&gt;

&lt;p&gt;Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs. The company reported 100% of treated subjects achieved complete viral elimination by day 7, with statistical significance of p=.001 versus placebo. No viral rebounds occurred during a 14-day post-treatment observation period.&lt;/p&gt;

&lt;p&gt;According to</description>
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   <title>Bioxytran reports viral clearance in phase 2 trial of ProLectin-M</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+viral+clearance+in+phase+2+trial+of+ProLectin-M/25979554.html</link>
   <description>

&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a Phase 2 trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo group participants.&lt;/p&gt;

&lt;p&gt;The randomized, double-blind, placebo-controlled trial enrolled 38 subjects with laboratory-confirmed acute viral infection. Participants received one of three ProLectin-M dose levels or placebo over seven days. All subjects completed the study.&lt;/p&gt;

&lt;p&gt;Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs. The company reported 100% of treated subjects achieved complete viral elimination by day 7, with statistical significance of p=.001 versus placebo. No viral rebounds occurred during a 14-day post-treatment observation period.&lt;/p&gt;

&lt;p&gt;According to</description>
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   <title>Bioxytran reports viral clearance in phase 2 trial of ProLectin-M</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+viral+clearance+in+phase+2+trial+of+ProLectin-M/25979554.html</link>
   <description>

&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a Phase 2 trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo group participants.&lt;/p&gt;

&lt;p&gt;The randomized, double-blind, placebo-controlled trial enrolled 38 subjects with laboratory-confirmed acute viral infection. Participants received one of three ProLectin-M dose levels or placebo over seven days. All subjects completed the study.&lt;/p&gt;

&lt;p&gt;Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs. The company reported 100% of treated subjects achieved complete viral elimination by day 7, with statistical significance of p=.001 versus placebo. No viral rebounds occurred during a 14-day post-treatment observation period.&lt;/p&gt;

&lt;p&gt;According to</description>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Feb 11</title>
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   <title>Form  8-K        BIOXYTRAN, INC            For: Feb 11</title>
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   <title>Bioxytran reports complete viral clearance in phase 2 antiviral trial</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+complete+viral+clearance+in+phase+2+antiviral+trial/25978409.html</link>
   <description>

&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a phase 2 clinical trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo. The randomized, double-blind, placebo-controlled study evaluated the company's ProLectin-M treatment in 38 subjects with laboratory-confirmed acute viral infection.&lt;/p&gt;

&lt;p&gt;The trial achieved statistical significance with a p-value of 0.001 for complete viral clearance at day 7. All 38 subjects completed the seven-day treatment period, receiving either one of three ProLectin-M dose levels or matching placebo. Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs, with clearance defined as non-detection of viral RNA below</description>
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   <pubDate>Wed, 11 Feb 2026 06:00:27 +0000</pubDate>
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   <title>Bioxytran reports complete viral clearance in phase 2 antiviral trial</title>
   <link>http://www.streetinsider.com/FDA/Bioxytran+reports+complete+viral+clearance+in+phase+2+antiviral+trial/25978409.html</link>
   <description>

&lt;p&gt;Bioxytran Inc. (OTCQB: BIXT) announced results from a phase 2 clinical trial showing complete elimination of viral load in all treated patients by day 7 compared to placebo. The randomized, double-blind, placebo-controlled study evaluated the company's ProLectin-M treatment in 38 subjects with laboratory-confirmed acute viral infection.&lt;/p&gt;

&lt;p&gt;The trial achieved statistical significance with a p-value of 0.001 for complete viral clearance at day 7. All 38 subjects completed the seven-day treatment period, receiving either one of three ProLectin-M dose levels or matching placebo. Viral clearance was measured using RT-PCR analysis of nasopharyngeal swabs, with clearance defined as non-detection of viral RNA below</description>
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