Telix Submits European Marketing Authorization Application for TLX101-Px

Reuters

02/18

Telix Submits European Marketing Authorization Application for TLX101-Px

Telix Pharmaceuticals Ltd. has submitted a marketing authorization application $(MAA)$ in Europe for TLX101-Px (O-(2-[18F]fluoroethyl)-L-tyrosine, 18F-FET), its glioma imaging candidate. The submission aims to expand access to advanced PET imaging for brain cancer in major European markets and follows alignment with U.S. FDA regulatory requirements. The U.S. New Drug Application (NDA) submission is planned to follow.

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. Telix Pharmaceuticals Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9656306-en) on February 17, 2026, and is solely responsible for the information contained therein.

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The submission aims to expand access to advanced PET imaging for brain cancer in major European markets and follows alignment with U.S. FDA regulatory requirements. The U.S. New Drug Application (NDA) submission is planned to follow.\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. Telix Pharmaceuticals Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: GNW9656306-en) on February 17, 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":"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:20260217:nNDL1kD1D0:1","article_id":"2612937114","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2612937114","pubTimestamp":1771365348,"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":"Telix Pharmaceuticals Ltd. has submitted a marketing authorization application  in Europe for TLX101-Px , its glioma imaging candidate. 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The submission aims to expand access to advanced PET imaging for brain cancer in major European markets and follows alignment with U.S. FDA regulatory requirements. The U.S. New Drug Application (NDA) submission is planned to follow.\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. Telix Pharmaceuticals Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. 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