CERo Therapeutics Initiates Dose Intensification in Phase 1 Trial of CER-1236 for Acute Myeloid Leukemia

Reuters

09/08

CERo <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Initiates Dose Intensification in Phase 1 Trial of CER-1236 for Acute Myeloid Leukemia

Cero Therapeutics Holdings Inc. has announced an update in the Phase 1 clinical trial of its drug candidate CER-1236, targeting patients with acute myeloid leukemia (AML). The company has intensified the dosing protocol for the study, administering a second dose to the second patient in the first cohort. This modification has been approved by the Institutional Review Board based on initial pharmacokinetic data indicating cell expansion. The aim is to assess the feasibility and safety of administering multiple infusions of CER-1236. The company plans to enroll a third patient in the cohort and anticipates that the protocol adjustment will yield valuable information regarding dosing, safety, and feasibility. Results from the trial have not yet been presented but are expected to provide insights as the study progresses.

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. Cero Therapeutics Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9524746-en) on September 08, 2025, and is solely responsible for the information contained therein.

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The company has intensified the dosing protocol for the study, administering a second dose to the second patient in the first cohort. This modification has been approved by the Institutional Review Board based on initial pharmacokinetic data indicating cell expansion. The aim is to assess the feasibility and safety of administering multiple infusions of CER-1236. The company plans to enroll a third patient in the cohort and anticipates that the protocol adjustment will yield valuable information regarding dosing, safety, and feasibility. Results from the trial have not yet been presented but are expected to provide insights as the study progresses.\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. Cero Therapeutics Holdings Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9524746-en) on September 08, 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":"LU2210149790.SGD","symbol_name":"Natixis Thematics Subscription Economy R/A SGD-H","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20250908:nNDL3DwFcx:1","article_id":"2565681498","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2565681498","pubTimestamp":1757335512,"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":"Cero Therapeutics Holdings Inc. has announced an update in the Phase 1 clinical trial of its drug candidate CER-1236, targeting patients with acute myeloid leukemia . 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The company has intensified the dosing protocol for the study, administering a second dose to the second patient in the first cohort. This modification has been approved by the Institutional Review Board based on initial pharmacokinetic data indicating cell expansion. The aim is to assess the feasibility and safety of administering multiple infusions of CER-1236. The company plans to enroll a third patient in the cohort and anticipates that the protocol adjustment will yield valuable information regarding dosing, safety, and feasibility. Results from the trial have not yet been presented but are expected to provide insights as the study progresses.\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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