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Use of the novel artificial intelligence–based test may provide a painless, low-cost alternative in bladder cancer screening.
AI-Based Urine Test Earns FDA Breakthrough Device Status in Bladder Cancer

July 1st 2025

Use of the novel artificial intelligence–based test may provide a painless, low-cost alternative in bladder cancer screening.

Detalimogene voraplasmid demonstrated a 71% any-time CR rate in this non-muscle invasive bladder cancer population in the phase 1/2 LEGEND trial.
FDA Grants RMAT Designation to Detalimogene in BCG-Unresponsive NMIBC

June 26th 2025

Data from the phase 3 ENVISION trial support the FDA approval of the mitomycin solution for patients with recurrent, low-grade, intermediate-risk NMIBC.
FDA Approves Mitomycin Solution in Low-Grade Intermediate-Risk NMIBC

June 12th 2025

Data from the ENVISION trial may support UGN-102 as a well-tolerated, efficacious treatment in non–muscle-invasive bladder cancer.
Robust Responses Occur With UGN-102 in Recurrent Intermediate-Risk NMIBC

June 11th 2025

Mitomycin/BCG Combo Shows Similar Efficacy, Reduced BCG Use in NMIBC
Mitomycin/BCG Combo Shows Similar Efficacy, Reduced BCG Use in NMIBC

June 3rd 2025

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