GT Biopharma erhält FDA-Zulassung für IND-Antrag zu GTB-5550

Reuters

Feb 03

GT Biopharma erhält FDA-Zulassung für IND-Antrag zu GTB-5550

GT Biopharma Inc. hat die Zulassung der US-amerikanischen FDA für die Durchführung einer Phase-1-Studie mit GTB-5550, einem B7-H3-gerichteten NK-Zell-Engager für solide Tumoren, erhalten. Die Studie ist als Basket-Studie konzipiert und soll voraussichtlich Mitte 2026 beginnen. Die Phase-1-Studie umfasst verschiedene solide Tumorarten mit B7-H3-Expression, wobei in der Dosiseskalationsphase insbesondere Patienten mit fortgeschrittenem Prostata-, Ovarial- und Pankreaskarzinom, die auf Standardtherapien nicht angesprochen haben, eingeschlossen werden.

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. GT Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 9647490) on February 03, 2026, and is solely responsible for the information contained therein.

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Die Studie ist als Basket-Studie konzipiert und soll voraussichtlich Mitte 2026 beginnen. Die Phase-1-Studie umfasst verschiedene solide Tumorarten mit B7-H3-Expression, wobei in der Dosiseskalationsphase insbesondere Patienten mit fortgeschrittenem Prostata-, Ovarial- und Pankreaskarzinom, die auf Standardtherapien nicht angesprochen haben, eingeschlossen werden.\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. GT Biopharma Inc. published the original content used to generate this news brief via GlobeNewswire (Ref. 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