Aardvark Therapeutics Receives IRB Approval for Expanded Phase 3 HERO Trial Eligibility

Reuters

Feb 10

<a href="https://laohu8.com/S/AARD">Aardvark Therapeutics</a> Receives IRB Approval for Expanded Phase 3 HERO Trial Eligibility

Aardvark Therapeutics Inc. announced that its amended protocol for the Phase 3 HERO clinical trial evaluating ARD-101 for the treatment of hyperphagia in individuals with Prader-Willi Syndrome has received Institutional Review Board (IRB) approval in the United States. The amended protocol, which was also submitted to the U.S. Food and Drug Administration (FDA), expands trial eligibility to include children as young as 7 years old, lowering the previous minimum age limit from 10 years. This change aims to broaden access to the trial for younger patients with Prader-Willi Syndrome.

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. Aardvark Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9651797-en) on February 10, 2026, and is solely responsible for the information contained therein.

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The amended protocol, which was also submitted to the U.S. Food and Drug Administration (FDA), expands trial eligibility to include children as young as 7 years old, lowering the previous minimum age limit from 10 years. This change aims to broaden access to the trial for younger patients with Prader-Willi Syndrome.\n      </p>\n</div><div xmlns:xsd=\"http://www.w3.org/2001/XMLSchema\" xmlns:xsi=\"http://www.w3.org/2001/XMLSchema-instance\">\n<p>\n<i>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. Aardvark Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9651797-en) on February 10, 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":"NDAQ","symbol_name":"纳斯达克OMX交易所","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260210:nNDLc9JY6T:1","article_id":"2610662883","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2610662883","pubTimestamp":1770728449,"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":"Aardvark Therapeutics Inc. announced that its amended protocol for the Phase 3 HERO clinical trial evaluating ARD-101 for the treatment of hyperphagia in individuals with Prader-Willi Syndrome has received Institutional Review Board  approval in the United States. 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The amended protocol, which was also submitted to the U.S. Food and Drug Administration (FDA), expands trial eligibility to include children as young as 7 years old, lowering the previous minimum age limit from 10 years. This change aims to broaden access to the trial for younger patients with Prader-Willi Syndrome.\n      \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. Aardvark Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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