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Clinical Trials in the EU / 2025-521277-14-00
Authorised, recruiting Phase II

A Phase 2 Multicenter, Open-Label Study Evaluating the Efficacy and Safety of TYRA-300 in Participants with FGFR3 Altered Low Grade, Intermediate Risk Non-Muscle Invasive Bladder Cancer (SURF302)

2025-521277-14-00 · tracked via the Priya Life Science EU tracker
Sponsor
Tyra Biosciences Inc
Sponsor type
Pharmaceutical company
Therapeutic area
Neoplasms
Decision date
08/10/2025
Enrollment target
42
Sites
Italy, Spain, France

Condition studied

Non-muscle invasive bladder cancer (NMIBC)

Eligibility

Age group
65+ years, 18-64 years
Sex
Female, Male

Primary endpoint

Complete response (CR) rate at 3 months

Endpoint detail

-Duration of response (responders only)., -Time to recurrence (responders only), -Recurrence-free survival rate at 12 months and 24 months (responders only), -Incidence and severity of adverse events, incidence of impact on study drug dosing, changes in clinical laboratory parameters, vital sign changes.

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 2025-521277-14-00 on CTIS ↗ ← All trials in the EU