Bioxytran Reports 100% Viral Clearance in Phase 2 Trial of ProLectin-M

Reuters

Feb 11

Bioxytran Reports 100% Viral Clearance in Phase 2 Trial of ProLectin-M

Bioxytran Inc. announced positive results from a recently completed Phase 2 randomized, double-blind, placebo-controlled, dose-optimization trial of ProLectin-M in subjects with laboratory-confirmed acute viral infection. The study enrolled 38 subjects and evaluated orally administered ProLectin-M over a seven-day treatment period. According to the company, the trial demonstrated complete elimination of viral load in 100% of treated subjects by Day 7 compared to placebo (p = .001), with a significant proportion achieving viral non-detection by Day 3. The results were presented by Bioxytran Inc., and the company plans to advance regulatory discussions and pursue late-stage clinical development of ProLectin-M for additional viral indications.

Disclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted as financial, investment, or legal advice. Bioxytran Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9652554) on February 11, 2026, and is solely responsible for the information contained therein.

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ID: 9652554) on February 11, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK4112","symbol_name":"金融交易所和数据","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260211:nNDLc6LqR8:1","article_id":"2610917936","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2610917936","pubTimestamp":1770807642,"columns":[],"sourceInfo":null,"weMediaInfo":{"media_name":"Reuters","introduction":"Reuters.com brings you the latest news from around the world, covering breaking news in markets, business, politics, entertainment and technology","home_visible":1,"id":"1032215980","head_image":"https://community-static.tradeup.com/news/4567337cbdf294b657b1fa87c5488b48"},"summary":"Bioxytran Inc. announced positive results from a recently completed Phase 2 randomized, double-blind, placebo-controlled, dose-optimization trial of ProLectin-M in subjects with laboratory-confirmed acute viral infection. 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While PUBT strives to provide accurate and timely information, this AI-generated content is for informational purposes only and should not be interpreted ","collect":0,"end_time":0,"defaultTopTitle":"","property":[],"viewcount":null,"language":"en","relate_stocks":{"BK4112":"金融交易所和数据","BK4585":"ETF&股票定投概念","IE00B3QW5Z07.USD":"GUINNESS GLOBAL MONEY MANAGERS \"C\" (USD) ACC","IE00BKPKM429.USD":"NEUBERGER BERMAN GLOBAL SUSTAINABLE EQUITY \"A\" (USD) ACC","LU2210150020.SGD":"Natixis Thematics Subscription Economy R/A SGD","BK4139":"生物科技","SG9999014021.USD":"UNITED GLOBAL DURABLE EQUITIES (USDHDG) ACC","IE00BGHQF748.EUR":"GUINNESS GLOBAL MONEY MANAGERS \"C\" (EUR) ACC","BIXT":"Bioxytran, Inc.","SG9999014005.SGD":"United Global Durable Equities Fund Acc SGD","LU2095319765.USD":"Natixis Thematics Subscription Economy R/A USD","NDAQ":"纳斯达克OMX交易所","IE00B64PRP62.GBP":"GUINNESS GLOBAL MONEY MANAGERS \"C\" (GBP) ACC","LU0314104364.USD":"MANULIFE GF AMERICAN GROWTH \"AA\" (USD) INC","SG9999014013.SGD":"United Global Durable Equities Fund Dis SGD","BK4588":"碎股","LU2210149790.SGD":"Natixis Thematics Subscription Economy R/A SGD-H","SG9999014039.USD":"UNITED GLOBAL DURABLE EQUITIES (USDHDG) INC"},"translate_title":"Bioxytran报告Prolectin-M 2期试验100%病毒清除","themeId":null,"isJumpTheme":false,"ttsUrl":null,"symbols_score_info":{"BIXT":0.9,"NDAQ":0.9},"content_text":"Bioxytran Reports 100% Viral Clearance in Phase 2 Trial of ProLectin-M\n    \n\n        Bioxytran Inc. announced positive results from a recently completed Phase 2 randomized, double-blind, placebo-controlled, dose-optimization trial of ProLectin-M in subjects with laboratory-confirmed acute viral infection. 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