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European agency recommends new Johnson & Johnson lung cancer treatment for advanced approval.
The European Medicines Agency's committee recommended Johnson & Johnson's subcutaneous form of Rybrevant (amivantamab) for patients with advanced EGFR-mutated non-small cell lung cancer.
This formulation reduces treatment time and infusion-related reactions compared to the intravenous form.
The recommendation follows successful phase 3 study results showing similar effectiveness.
If approved, it could offer a more convenient treatment option for patients.
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La agencia europea recomienda un nuevo tratamiento para el cáncer de pulmón de Johnson & Johnson para su aprobación avanzada.