Tevogen Bio Expands Precision T Cell Therapy Eligibility With Multi-HLA Targeting

Reuters

2025/11/06

Tevogen Bio Expands Precision T Cell Therapy Eligibility With Multi-HLA Targeting

Tevogen Bio Holdings Inc. has announced a significant clinical milestone in the development of its investigational precision T cell therapy, TVGN 489, designed for the treatment of acute and Long COVID. The company has completed T cell target identification for an additional five human leukocyte antigen (HLA) restrictions, broadening patient eligibility for its therapy. This advancement builds on a previously completed clinical trial of TVGN 489, which demonstrated 100% viral clearance, no reinfections, and no cases of Long COVID in high-risk patients. Results from this initial proof-of-concept trial were published in Blood Advances. TVGN 489 utilizes off-the-shelf, genetically unmodified allogeneic T cells and aims to expand therapeutic access regardless of patients' genetic backgrounds.

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. Tevogen Bio Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9569710-en) on November 05, 2025, and is solely responsible for the information contained therein.

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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 as financial, investment, or legal advice. <a href=\"https://laohu8.com/S/TVGN\">Tevogen Bio Holdings</a> Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9569710-en) on November 05, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"LU2095319765.USD","symbol_name":"Natixis Thematics Subscription Economy R/A USD","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251105:nNDL3blB8C:1","article_id":"2581706505","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2581706505","pubTimestamp":1762374018,"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":"Tevogen Bio Holdings Inc. has announced a significant clinical milestone in the development of its investigational precision T cell therapy, TVGN 489, designed for the treatment of acute and Long COVID. The company has completed T cell target identification for an additional five human leukocyte antigen  restrictions, broadening patient eligibility for its therapy. This advancement builds on a previously completed clinical trial of TVGN 489, which demonstrated 100% viral clearance, no reinfections, and no cases of Long COVID in high-risk patients. Results from this initial proof-of-concept trial were published in Blood Advances. TVGN 489 utilizes off-the-shelf, genetically unmodified allogeneic T cells and aims to expand therapeutic access regardless of patients' genetic backgrounds.Disclaimer: This news brief was created by Public Technologies  using generative artificial intelligence. 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The company has completed T cell target identification for an additional five human leukocyte antigen (HLA) restrictions, broadening patient eligibility for its therapy. This advancement builds on a previously completed clinical trial of TVGN 489, which demonstrated 100% viral clearance, no reinfections, and no cases of Long COVID in high-risk patients. Results from this initial proof-of-concept trial were published in Blood Advances. TVGN 489 utilizes off-the-shelf, genetically unmodified allogeneic T cells and aims to expand therapeutic access regardless of patients' genetic backgrounds.\n      \n\nDisclaimer: 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. 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