Vir Biotechnology Reports Positive Phase 2 Results for Tobevibart and Elebsiran in Hepatitis Delta

Reuters

2025/11/10

<a href="https://laohu8.com/S/VIR">Vir Biotechnology</a> Reports Positive Phase 2 Results for Tobevibart and Elebsiran in Hepatitis Delta

Vir Biotechnology Inc. announced results from its Phase 2 SOLSTICE trial evaluating the combination of tobevibart and elebsiran for the treatment of chronic hepatitis delta $(CHD)$. Data presented at The Liver Meeting® of the American Association for the Study of Liver Diseases (AASLD) and published in the New England Journal of Medicine showed that 66% of participants receiving a monthly dose of the combination achieved undetectable hepatitis delta virus $(HDV)$ RNA at Week 48. The combination was well-tolerated, with no grade 3 or higher treatment-related adverse events and no treatment-related discontinuations reported. The ECLIPSE registrational program for the combination therapy is underway, with topline data expected in the first quarter of 2027. The combination has received Breakthrough Therapy and Fast Track designations from the U.S. Food and Drug Administration, as well as Priority Medicines and orphan drug designations from the European Medicines Agency.

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. Vir Biotechnology Inc. published the original content used to generate this news brief on November 09, 2025, and is solely responsible for the information contained therein.

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Data presented at The Liver Meeting® of the American Association for the Study of Liver Diseases (AASLD) and published in the <a href=\"https://laohu8.com/S/NEWEN\">New England</a> Journal of Medicine showed that 66% of participants receiving a monthly dose of the combination achieved undetectable hepatitis delta virus <a href=\"https://laohu8.com/S/HDV\">$(HDV)$</a> RNA at Week 48. The combination was well-tolerated, with no grade 3 or higher treatment-related adverse events and no treatment-related discontinuations reported. The ECLIPSE registrational program for the combination therapy is underway, with topline data expected in the first quarter of 2027. 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Vir Biotechnology Inc. published the original content used to generate this news brief on November 09, 2025, and is solely responsible for the information contained therein.</span></em>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"BK4535","symbol_name":"淡馬錫持倉","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251109:nNDL6LFr4f:1","article_id":"2582581952","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2582581952","pubTimestamp":1762729801,"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":"Vir Biotechnology Inc. announced results from its Phase 2 SOLSTICE trial evaluating the combination of tobevibart and elebsiran for the treatment of chronic hepatitis delta . 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Data presented at The Liver Meeting® of the American Association for the Study of Liver Diseases (AASLD) and published in the New England Journal of Medicine showed that 66% of participants receiving a monthly dose of the combination achieved undetectable hepatitis delta virus $(HDV)$ RNA at Week 48. The combination was well-tolerated, with no grade 3 or higher treatment-related adverse events and no treatment-related discontinuations reported. The ECLIPSE registrational program for the combination therapy is underway, with topline data expected in the first quarter of 2027. The combination has received Breakthrough Therapy and Fast Track designations from the U.S. Food and Drug Administration, as well as Priority Medicines and orphan drug designations from the European Medicines Agency.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. 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