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The FDA approves zongertinib for adults with HER2-mutated lung cancer, showing a 75% response rate.
The FDA has granted accelerated approval to zongertinib (Hernexeos) for adults with certain types of non-small cell lung cancer (NSCLC) that have HER2 mutations and who have received prior treatment.
The drug showed a 75% overall response rate in clinical trials and offers a new targeted treatment option for patients with this condition.
The FDA also approved a companion diagnostic test to identify suitable patients.
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La FDA aprueba zongertinib para adultos con cáncer de pulmón con mutación HER2, mostrando una tasa de respuesta del 75%.