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The FDA grants priority review for a new lung cancer drug, taletrectinib, aiming for approval by June 2025.
The FDA has granted a priority review for Nuvation Bio's application for taletrectinib, a new drug for advanced ROS1-positive non-small cell lung cancer.
The approval process, which aims to expedite the availability of potential new therapies, is targeted for completion by June 23, 2025.
The decision is based on data from Phase 2 studies, and Nuvation Bio's stock saw a 4.43% increase in pre-market trading.
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La FDA concede una revisión prioritaria para un nuevo medicamento contra el cáncer de pulmón, taletrectinib, con el objetivo de su aprobación para junio de 2025.