Kalaris Therapeutics Unveils Phase 1 Data for TH103 in Neovascular AMD at Macula Society Meeting

Reuters

01/29

Kalaris <a href="https://laohu8.com/S/LENZ">Therapeutics</a> Unveils Phase 1 Data for TH103 in Neovascular <a href="https://laohu8.com/S/AMD">AMD</a> at Macula Society Meeting

Kalaris Therapeutics Inc. announced that clinical data from its Phase 1 study of TH103, a novel dual-targeting VEGF and HSPG inhibitor, will be presented at the 49th Annual Meeting of the Macula Society. The presentation is scheduled for February 26, 2026, in San Diego, California, and will cover safety, tolerability, pharmacokinetics, and early efficacy outcomes following intravitreal administration of TH103 in patients with treatment-naive neovascular age-related macular degeneration. The results have not yet been presented.

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. Kalaris Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9644579) on January 28, 2026, and is solely responsible for the information contained therein.

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The presentation is scheduled for February 26, 2026, in San Diego, California, and will cover safety, tolerability, pharmacokinetics, and early efficacy outcomes following intravitreal administration of TH103 in patients with treatment-naive neovascular age-related macular degeneration. The results have not yet been presented.\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. Kalaris Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9644579) on January 28, 2026, and is solely responsible for the information contained therein.</span></i>\n</p>\n</div></body></html>\n</article>\n</div>\n</body>\n</html>\n","isBrief":false,"type":0,"news_type":1,"symbol":"KLRS","symbol_name":"Kalaris Therapeutics Inc.","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260128:nNDL5vPbtk:1","article_id":"2607740698","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2607740698","pubTimestamp":1769634334,"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":"Kalaris Therapeutics Inc. announced that clinical data from its Phase 1 study of TH103, a novel dual-targeting VEGF and HSPG inhibitor, will be presented at the 49th Annual Meeting of the Macula Society. 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The presentation is scheduled for February 26, 2026, in San Diego, California, and will cover safety, tolerability, pharmacokinetics, and early efficacy outcomes following intravitreal administration of TH103 in patients with treatment-naive neovascular age-related macular degeneration. The results have not yet been presented.\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. Kalaris Therapeutics Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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