FDA revisa TEV-749 de Teva; decisión prevista en 4T 2026
- Teva espera una decisión de la FDA en el 4T 2026 sobre TEV-749, su olanzapina inyectable mensual subcutánea para esquizofrenia.
- La EMA aceptó en mayo de 2026 la solicitud de autorización de comercialización en la UE para TEV-749.
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. Teva Pharmaceutical Industries Ltd. published the original content used to generate this news brief via GlobeNewswire (Ref. ID: 202609181630PRIMZONEFULLFEED1001263355) on September 18, 2026, and is solely responsible for the information contained therein.