Nuvation Bio and Eisai Receive EMA Validation for Taletrectinib Treatment in Europe
ByAinvest
Wednesday, Apr 1, 2026 7:12 am ET1min read
NUVB--
Nuvation Bio Inc. (NUVB) and Eisai announced that the European Medicines Agency (EMA) validated the Marketing Authorisation Application (MAA) for Taletrectinib, a treatment for advanced ROS1-positive non-small cell lung cancer. Management expects a standard review timeline and notes that Europe sees around 400,000 annual lung cancer diagnoses, with non-small cell lung cancer comprising 80%.
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