Radiopharm Theranostics doses first patient in Phase 1/2a trial of 177Lu-BetaBart (RV-01)

Reuters

02/26

<a href="https://laohu8.com/S/RDPTF">Radiopharm Theranostics</a> doses first patient in Phase 1/2a trial of 177Lu-BetaBart (RV-01)

Radiopharm Theranostics Ltd. announced it has dosed the first patient in its first-in-human Phase 1/2a clinical trial of 177Lu-BetaBart (RV-01). The dose escalation and expansion study is designed to evaluate safety, biodistribution and radiation dosimetry, as well as preliminary anti-tumor activity, and to determine a recommended dose for future studies. The company also referenced preclinical animal studies reporting tumor shrinkage and prolonged survival, and noted that the FDA provided IND clearance for Betabart (RV-01) on 28 July 2025.

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. Radiopharm Theranostics Ltd. published the original content used to generate this news brief on February 25, 2026, and is solely responsible for the information contained therein.

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The dose escalation and expansion study is designed to evaluate safety, biodistribution and radiation dosimetry, as well as preliminary anti-tumor activity, and to determine a recommended dose for future studies. The company also referenced preclinical animal studies reporting tumor shrinkage and prolonged survival, and noted that the FDA provided IND clearance for Betabart (RV-01) on 28 July 2025.\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. Radiopharm Theranostics Ltd. published the original content used to generate this news brief on February 25, 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":"RAD.AU","symbol_name":"RADIOPHARM THERANOSTICS LTD","start_time":0,"source_url":"https://api.refinitiv.com/data/news/v1/stories/urn:newsml:reuters.com:20260225:nNDL5tbjXL:1","article_id":"2614580250","we_media_id":"1032215980","thumbnails":[],"rights":null,"url":"https://stock-news.laohu8.com/highlight/detail?id=2614580250","pubTimestamp":1772049034,"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":"Radiopharm Theranostics Ltd. announced it has dosed the first patient in its first-in-human Phase 1/2a clinical trial of 177Lu-BetaBart . 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