FDA acepta revisión prioritaria de sac-TMT de Merck para cáncer de endometrio
- La FDA aceptó para revisión prioritaria la solicitud de aprobación de sacituzumab tirumotecan de Merck para cáncer de endometrio.
- La solicitud abarca adultos previamente tratados con quimioterapia con platino e inhibidores de PD-1 o PD-L1, por separado o combinados.
- La fecha objetivo para la decisión regulatoria es el 15 de junio de 2027.
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. Merck & Co. Inc. published the original content used to generate this news brief via Business Wire (Ref. ID: 20261026572930) on October 26, 2026, and is solely responsible for the information contained therein.