Clinical Trials in the EU / 2026-526359-75-00
Authorised, recruiting
Phase IV
A Rollover Study to Follow the Long-term Durability of Response to UGN-103 in Participants From Study BL013
2026-526359-75-00 · tracked via the Priya Life Science EU tracker
Condition studied
Non-Muscle Invasive Bladder Cancer
Investigational medicinal product(s)
UGN-103 (Mitomycin)
Eligibility
Primary endpoint
Duration of response (DOR)
Official registry record
This page summarises publicly available CTIS data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View 2026-526359-75-00 on CTIS ↗ ← All trials in the EU