Johnson & Johnson's subsidiary, Janssen-Cilag International, has received European Commission approval for its oncology drug, BALVERSA (erdafitinib). It is designed to treat adults suffering from urothelial carcinoma (mUC) that cannot be removed via surgery or has metastasized.
BALVERSA is an oral monotherapy designed to be taken once daily. It's formulated for patients with mUC who have certain FGFR3 genetic alterations and have undergone at least one treatment that involved either a PD-1 or PD-L1 inhibitor. The company claims that according to trial data, patients on erdafitinib had a median overall survival of over a year, with disease progression-free survival of 5.6 months compared to 2.7 months with chemotherapy.
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