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FDA approves Inlexzo, a new bladder cancer treatment showing over 80% patient response rate.
The FDA has approved Inlexzo, a new treatment for adults with BCG-unresponsive non-muscle-invasive bladder cancer with carcinoma in situ, with or without papillary tumors.
Inlexzo is the first intravesical drug-releasing system that provides extended local delivery of the drug gemcitabine directly into the bladder.
Based on clinical study data, over 80% of patients achieved a complete response, with more than half maintaining this response for at least a year.
Approval was granted to Johnson & Johnson.
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La FDA aprueba Inlexzo, un nuevo tratamiento para el cáncer de vejiga que muestra una tasa de respuesta del 80% en los pacientes.