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Completed Phase 2 Interventional

Phase 2 Study of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) (Enlarged Prostate)

ClinicalTrials.gov ID: NCT00759135

Public ClinicalTrials.gov record NCT00759135. 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 Jul 23, 2026, 8:06 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

Phase 2 Multicenter Randomized Two Dose Level and Non-Inferiority Clinical Evaluation of Transrectal Administration of NX-1207 for the Treatment of BPH

Study identification

NCT ID
NCT00759135
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Nymox Corporation
Industry
Enrollment
85 participants

Conditions and interventions

Interventions

  • 2.5 mg NX-1207 Drug
  • 0.125 mg NX-1207 Drug
  • finasteride Drug

Drug

Eligibility (public fields only)

Age range
45 Years to 75 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
Apr 30, 2007
Primary completion
Dec 31, 2007
Completion
Apr 30, 2008
Last update posted
Jun 13, 2012

2007 – 2008

United States locations

U.S. sites
30
U.S. states
17
U.S. cities
30
Facility City State ZIP Site status
Nymox Investigational Site Huntsville Alabama
Nymox Investigational Site Tucson Arizona
Nymox Investigational Site Little Rock Arkansas
Nymox Investigational Site Anaheim California
Nymox Investigational Site Atherton California
Nymox Investigational Site Long Beach California
Nymox Investigational Site Modesto California
Nymox Investigational Site Newport Beach California
Nymox Investigational Site Denver Colorado
Nymox Investigational Site New Britain Connecticut
Nymox Investigational Site Sarasota Florida
Nymox Investigational Site Greenwood Indiana
Nymox Investigational Site Jeffersonville Indiana
Nymox Investigational Site Shreveport Louisiana
Nymox Investigational Site Missoula Montana
Nymox Investigational Site Las Vegas Nevada
Nymox Investigational Site Lawrenceville New Jersey
Nymox Investigational Site Marlton New Jersey
Nymox Investigational Site Voorhees Township New Jersey
Nymox Investigational Site Garden City New York
Nymox Investigational Site Poughkeepsie New York
Nymox Investigational Site Staten Island New York
Nymox Investigational Site Lancaster Pennsylvania
Nymox Investigational Site Myrtle Beach South Carolina
Nymox Investigational Site Germantown Tennessee
Nymox Investigational Site Arlington Texas
Nymox Investigational Site Brownsville Texas
Nymox Investigational Site Dallas Texas
Nymox Investigational Site McAllen Texas
Nymox Investigational Site San Antonio Texas

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 NCT00759135, 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 Jun 13, 2012 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00759135 live on ClinicalTrials.gov.

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