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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00918983
Other study ID # NX02-0017
Secondary ID
Status Completed
Phase Phase 3
First received June 9, 2009
Last updated April 1, 2014
Start date April 2009
Est. completion date November 2013

Study information

Verified date April 2014
Source Nymox Corporation
Contact n/a
Is FDA regulated No
Health authority United States: Food and Drug Administration
Study type Interventional

Clinical Trial Summary

This study will evaluate the safety and efficacy of a 2.5 mg dose of NX-1207 for the treatment of BPH (benign prostatic hyperplasia) as compared to placebo.


Recruitment information / eligibility

Status Completed
Enrollment 500
Est. completion date November 2013
Est. primary completion date November 2013
Accepts healthy volunteers No
Gender Male
Age group 45 Years and older
Eligibility Inclusion Criteria:

1. Provide signed informed consent prior to enrolment in the study

2. IPSS = 15

3. Prostate Volume = 30 mL = 70 mL

4. Qmax < 15 mL/sec based on a minimum void of 125 mL

5. Agree not to use any other approved or experimental BPH or OAB medication anytime during the study

Exclusion Criteria:

1. History of illness or condition that may interfere with study or endanger subject

2. Use of prescribed medications that may interfere with study or endanger subject

3. Presence of a median lobe of the prostate

4. Previous surgery or MIST for treatment of BPH

5. Post-void residual urine volume > 200 mL

6. PSA = 10 ng/mL; prostate cancer must be ruled out (negative biopsy) for PSA = 4 ng/mL

7. Participation in a study of any investigational drug or device within the previous 90 days

8. Prostate cancer

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Investigator), Primary Purpose: Treatment


Intervention

Drug:
NX-1207
Single intraprostatic injection of 2.5 mg NX-1207
Placebo
Single intraprostatic injection of placebo

Locations

Country Name City State
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Anaheim California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Arlington Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Atherton California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669 Atlanta Georgia
United States For information concerning this clinical site, please contact Nymox at 800-936-9669 Bala Cynwyd Pennsylvania
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Bethany Oklahoma
United States For information concerning this clinical site, please contact Nymox at 800-936-9669 Birmingham Alabama
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Brooklyn New York
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Carrollton Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Cincinnati Ohio
United States For information concerning this clinical site, please contact Nymox at 800-936-9669 Columbus Ohio
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Concord North Carolina
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Dallas Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Denver Colorado
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Garden City New York
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Huntsville Alabama
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Jeffersonville Indiana
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Knoxville Tennessee
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. La Mesa California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Lancaster Pennsylvania
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Lawrenceville New Jersey
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Little Rock Arkansas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Long Beach California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Los Alamitos California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Missoula Montana
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Mt. Laurel New Jersey
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Myrtle Beach South Carolina
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Naples Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. New Britain Connecticut
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Newburg Indiana
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Ocala Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Orlando Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Poughkeepsie New York
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Raleigh North Carolina
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Roswell Georgia
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Salem Oregon
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Salt Lake City Utah
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Shreveport Louisiana
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Tallahassee Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Tucson Arizona
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Voorhees New Jersey

Sponsors (1)

Lead Sponsor Collaborator
Nymox Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary International Prostate Symptom Score (IPSS) 365 days No
Secondary International Prostate Symptom Score (IPSS) 90 days No
Secondary International Prostate Symptom Score (IPSS) 180 days No
Secondary International Prostate Symptom Score (IPSS) 270 days No
Secondary Peak urine flow rate (Qmax) 365 days No
Secondary Peak urine flow rate (Qmax) 90 days No
Secondary Peak urine flow rate (Qmax) 180 days No
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