Study of PRX302 for Lower Urinary Tract Symptoms Due to Benign Prostatic Hyperplasia (BPH)
Public ClinicalTrials.gov record NCT01454349. 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
A Randomized Dose-Escalation, Multicenter Safety and Efficacy Study of a Single Transrectal Intraprostatic Treatment of PRX302 for Lower Urinary Tract Symptoms (LUTS) Secondary to Benign Prostatic Hyperplasia (BPH)
Study identification
- NCT ID
- NCT01454349
- Recruitment status
- Completed
- Study type
- Interventional
- Phase
- Phase 1, Phase 2
- Lead sponsor
- Sophiris Bio Corp
- Industry
- Enrollment
- 40 participants
Conditions and interventions
Conditions
Interventions
- PRX302 Drug
- Placebo Drug
Drug
Eligibility (public fields only)
- Age range
- 50 Years to 80 Years
- Sex
- Male
- 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
- Aug 31, 2011
- Primary completion
- Feb 28, 2013
- Completion
- Jul 31, 2013
- Last update posted
- Aug 20, 2013
2011 – 2013
United States locations
- U.S. sites
- 15
- U.S. states
- 10
- U.S. cities
- 15
| Facility | City | State | ZIP | Site status |
|---|---|---|---|---|
| South Orange County Medical Research Center | Laguna Hills | California | 92653 | — |
| Atlantic Urology Medical Group | Long Beach | California | 90806 | — |
| California Professional Research | Newport Beach | California | 92660 | — |
| University of Colorado Denver | Aurora | Colorado | 80045 | — |
| South Florida Medical Research | Aventura | Florida | 33180 | — |
| Northwestern University | Chicago | Illinois | 60611 | — |
| The Iowa Clinic | West Des Moines | Iowa | 50266 | — |
| Accumed Research Associates | Garden City | New York | 11530 | — |
| University Urology Associates | New York | New York | 10016 | — |
| Premier Medical Group of the Hudson Valley | Poughkeepsie | New York | 12601 | — |
| TriState Urological Services | Cincinnatti | Ohio | 45212 | — |
| Urologic Consultants of SE Pennsylvania | Bala-Cynwyd | Pennsylvania | 19004 | — |
| Carolina Urologic Research Center | Myrtle Beach | South Carolina | 29572 | — |
| Research Across America | Carrollton | Texas | 75010 | — |
| UT Southwestern Medical Center | Dallas | Texas | 75390 | — |
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 NCT01454349, 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 Aug 20, 2013 · Synced Jul 23, 2026
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Open the official record
The complete protocol, eligibility criteria, and contact information for NCT01454349 live on ClinicalTrials.gov.