Revelation Biosciences Advances Gemini Toward FDA Review for Acute Kidney Injury

Reuters

2025/11/20

<a href="https://laohu8.com/S/REVBU">Revelation Biosciences</a> Advances Gemini Toward FDA Review for Acute Kidney Injury

Revelation Biosciences Inc. announced the successful submission and acceptance of its end-of-phase 1 meeting package to the FDA for Gemini, its investigational treatment for acute kidney injury (AKI). The company is on track to hold the regulatory meeting with the FDA later this year. This meeting will focus on establishing agency feedback and input for the clinical development and regulatory approval pathway for Gemini. There was no announcement regarding grant or funding obtained by Revelation Biosciences Inc. or any other organizations.

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. Revelation Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1105050) on November 20, 2025, and is solely responsible for the information contained therein.

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The company is on track to hold the regulatory meeting with the FDA later this year. This meeting will focus on establishing agency feedback and input for the clinical development and regulatory approval pathway for Gemini. There was no announcement regarding grant or funding obtained by <a href=\"https://laohu8.com/S/REVBW\">Revelation Biosciences</a> Inc. or any other organizations.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<em>Disclaimer: <span>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. Revelation Biosciences Inc. published the original content used to generate this news brief via ACCESS Newswire (Ref. ID: 1105050) on November 20, 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":"REVB","symbol_name":"Revelation Biosciences, Inc.","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20251120:nNDL7BNX7w:1","article_id":"2584137369","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2584137369","pubTimestamp":1763647223,"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":"Revelation Biosciences Inc. announced the successful submission and acceptance of its end-of-phase 1 meeting package to the FDA for Gemini, its investigational treatment for acute kidney injury . 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