Nuvation Bio shares rise; EMA validates taletrectinib MAA for advanced ROS1+ NSCLC in Europe

Reuters03-27

<a href="https://laohu8.com/S/NUVB">Nuvation Bio</a> shares rise; EMA validates taletrectinib MAA for advanced ROS1+ NSCLC in Europe

The European Medicines Agency validated and accepted for review a Marketing Authorisation Application for taletrectinib to treat advanced ROS1+ non-small cell lung cancer.
Eisai and Nuvation Bio said the application will follow a standard review timeline.
Taletrectinib is already approved in the US, China, and Japan for advanced ROS1+ non-small cell lung cancer.

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. Nuvation Bio Inc. published the original content used to generate this news brief on March 26, 2026, and is solely responsible for the information contained therein.

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