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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

Detalimogene voraplasmid demonstrated a 71% any-time CR rate in this non-muscle invasive bladder cancer population in the phase 1/2 LEGEND trial.

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

Sasanlimab Combo Poised to Change High-Risk NMIBC Treatment Paradigm
Sasanlimab Combo Poised to Change High-Risk NMIBC Treatment Paradigm

May 31st 2025

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