Balversa® (erdafitinib) – Updated indication, accelerated approval converted to full approval
January 19, 2024 - Johnson & Johnson announced the full FDA approval of Balversa (erdafitinib), for the treatment of adult patients with locally advanced or metastatic urothelial carcinoma (mUC) with susceptible FGFR3 genetic alterations whose disease has progressed on or after at least one line of prior systemic therapy.