URO-902 in Female Subjects With Overactive Bladder and Urge Urinary Incontinence
Public ClinicalTrials.gov record NCT04211831. 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.
Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.
Official title
An Exploratory Phase 2a Study Evaluating the Efficacy and Safety of URO-902 in Subjects With Overactive Bladder and Urge Urinary Incontinence
Brief summary
Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.
This study will evaluate the efficacy, safety, and tolerability of a single dose of URO-902 24 milligrams (mg) and 48 mg (administered via intradetrusor injection), compared with placebo, in participants with overactive bladder (OAB) and urge urinary incontinence (UUI) up to 48 weeks post-dose.
Study identification
- NCT ID
- NCT04211831
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 2
- Enrollment
- 80 participants
Conditions and interventions
Eligibility (public fields only)
- Age range
- 40 Years to 79 Years
- Sex
- Female
- 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
- Dec 15, 2019
- Primary completion
- Nov 17, 2021
- Completion
- Jul 19, 2022
- Last update posted
- Apr 19, 2023
2019 – 2022
United States locations
- U.S. sites
- 20
- U.S. states
- 14
- U.S. cities
- 20
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| Coastal Clinical Research Inc | Mobile | Alabama | 36608 | — |
| Urological Associates of Southern Arizona | Tucson | Arizona | 85715 | — |
| Orange County Urology Associates | Laguna Hills | California | 92653 | — |
| University of Southern California - Norris Hospital | Los Angeles | California | 90033 | — |
| Tri Valley Urology Medical Group | Murrieta | California | 92562 | — |
| Stanford University School of Medicine | Palo Alto | California | 94304 | — |
| Precision Clinical Research LLC | Sunrise | Florida | 33351 | — |
| Iowa Clinic | West Des Moines | Iowa | 50266 | — |
| Chesapeake Urology Associates | Hanover | Maryland | 21076 | — |
| Bay State Clinical Trials | Watertown | Massachusetts | 02472 | — |
| Beaumont Hospital | Royal Oak | Michigan | 48073 | — |
| Premier Urology Group, LLC | Edison | New Jersey | 08837 | — |
| Urology Center of Englewood | Englewood | New Jersey | 07631 | — |
| Great Lakes Physician PC / Western New York Urology Associates | Cheektowaga | New York | 14225 | — |
| Accumed Research Associates - ClinEdge - PPDS | Garden City | New York | 11530 | — |
| Atrium Healthcare | Charlotte | North Carolina | 28203 | — |
| Urology Specialists of The Carolinas | Huntersville | North Carolina | 28078 | — |
| Institute For Female Pelvic Medicine | Allentown | Pennsylvania | 18104 | — |
| Urology of Virginia | Virginia Beach | Virginia | 23462 | — |
| Washington Urology & Urogynecology Associates | Kirkland | Washington | 98034 | — |
Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.
About this trial record page
- What this page shows
- Public field values for ClinicalTrials.gov record NCT04211831, 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 Apr 19, 2023 · Synced Sep 4, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT04211831 live on ClinicalTrials.gov.