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Completed Phase 2 Interventional Results available

A Phase 2b Study of UGN-102 for Low Grade Intermediate Risk Non-Muscle-Invasive Bladder Cancer

ClinicalTrials.gov ID: NCT03558503

Public ClinicalTrials.gov record NCT03558503. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 2:29 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 2b, Single-Arm, Multicenter Trial to Evaluate the Efficacy and Safety of UGN-102 as Primary Chemoablative Therapy in Patients With Low Grade (LG) Non-Muscle-Invasive Bladder Cancer (NMIBC) at Intermediate Risk of Recurrence

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This Phase 2b, single-arm, multicenter study evaluated the efficacy and safety of UGN-102 as primary chemoablative therapy in patients with low grade intermediate risk non-muscle-invasive bladder cancer (LG IR NMIBC).

Study identification

NCT ID
NCT03558503
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
UroGen Pharma Ltd.
Industry
Enrollment
63 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 15, 2018 (Actual)
Primary completion
Jan 3, 2020 (Actual)
Completion
Oct 21, 2020 (Actual)
Last update posted
Sep 16, 2022

2018 – 2020

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
14
Facility City State ZIP Site status
Mayo Clinic Cancer Center Phoenix Arizona 85054 —
Arkansas Urology Little Rock Arkansas 72211 —
Loma Linda University Loma Linda California 92350 —
Providence Medical Institute Santa Monica California 90404 —
Clinical Research Center of Florida Pompano Beach Florida 33060 —
John Hopkins University Baltimore Maryland 21218 —
Adult & Pediatric Urology, PC Omaha Nebraska 68114 —
Urology Las Vegas Las Vegas Nevada 89144 —
Manhattan Medical Research New York New York 10016 —
Weill Cornell Medical College New York New York 10065 —
Montefiore Medical Center (Albert Einstein) New York New York 10461 —
Western New York Urology Associates New York New York 14225 —
The University of North Carolina Chapel Hill North Carolina 27572 —
Penn State Hershey State College Hershey Pennsylvania 17033 —
Carolina Urologic Research Center Myrtle Beach South Carolina 29572 —
Urology Associates, PC Nashville Tennessee 37209 —
Urology San Antonio Fredericksburg Texas 78233 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 2 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03558503, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Sep 16, 2022 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03558503 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →