Invivyd Receives FDA Clearance to Advance Pivotal Clinical Trials for VYD2311, a Monoclonal Antibody COVID-19 Vaccine Alternative

Reuters

Oct 06

Invivyd Receives FDA Clearance to Advance Pivotal Clinical Trials for VYD2311, a Monoclonal Antibody COVID-19 Vaccine Alternative

Invivyd Inc. (Nasdaq: IVVD) announced on October 6, 2025, that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VYD2311, a monoclonal antibody candidate developed as a vaccine alternative for the prevention of COVID-19. This regulatory milestone allows Invivyd to advance its REVOLUTION clinical program, including the pivotal DECLARATION and LIBERTY trials, which are expected to begin by the end of 2025. Invivyd has produced commercial launch quantities of VYD2311 and secured funding to support clinical trial execution through to pivotal data readouts. No other organizations were mentioned as recipients of grant or funding in this announcement.

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. Invivyd Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9540330-en) on October 06, 2025, and is solely responsible for the information contained therein.

Disclaimer: Investing carries risk. This is not financial advice. The above content should not be regarded as an offer, recommendation, or solicitation on acquiring or disposing of any financial products, any associated discussions, comments, or posts by author or other users should not be considered as such either. It is solely for general information purpose only, which does not consider your own investment objectives, financial situations or needs. TTM assumes no responsibility or warranty for the accuracy and completeness of the information, investors should do their own research and may seek professional advice before investing.

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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. Invivyd Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9540330-en) on October 06, 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":"IE00B3QW5Z07.USD","symbol_name":"GUINNESS GLOBAL MONEY MANAGERS \"C\" (USD) ACC","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251006:nNDL70zn6Y:1","article_id":"2573967996","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2573967996","pubTimestamp":1759748477,"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":"Invivyd Receives FDA Clearance to Advance Pivotal Clinical Trials for VYD2311, a Monoclonal Antibody COVID-19 Vaccine Alternative. 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(Nasdaq: IVVD) announced on October 6, 2025, that the U.S. Food and Drug Administration (FDA) has cleared its Investigational New Drug (IND) application for VYD2311, a monoclonal antibody candidate developed as a vaccine alternative for the prevention of COVID-19. This regulatory milestone allows Invivyd to advance its REVOLUTION clinical program, including the pivotal DECLARATION and LIBERTY trials, which are expected to begin by the end of 2025. Invivyd has produced commercial launch quantities of VYD2311 and secured funding to support clinical trial execution through to pivotal data readouts. No other organizations were mentioned as recipients of grant or funding in this announcement.\n      \n\nDisclaimer: This news brief was created by Public Technologies (PUBT) using generative artificial intelligence. 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