Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00945490
Other study ID # NX02-0018
Secondary ID
Status Completed
Phase Phase 3
First received July 22, 2009
Last updated March 9, 2017
Start date May 2009
Est. completion date May 2014

Study information

Verified date March 2017
Source Nymox Corporation
Contact n/a
Is FDA regulated No
Health authority
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 May 2014
Est. primary completion date May 2014
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. AUASI = 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


Related Conditions & MeSH terms


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. Albany New York
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Albuquerque New Mexico
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Annapolis Maryland
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Aventura Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Baltimore Maryland
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Bismarck North Dakota
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Brick New Jersey
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Bryn Mawr Pennsylvania
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. Englewood 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. Glen Burnie Maryland
United States For information concerning this clinical site, please contact Nymox at 800-936-9669 Grand Rapids Michigan
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Houston Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Laguna Hills California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Las Vegas Nevada
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Las Vegas Nevada
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. McAllen Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Memphis Tennessee
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Meridian Idaho
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. New York New York
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. Oklahoma City Oklahoma
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. Richmond Virginia
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. San Antonio Texas
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. San Diego California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. San Diego California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Sarasota Florida
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Sartell Minnesota
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Sewickley Pennsylvania
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Southaven Mississippi
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Tarzana California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Torrance California
United States For information concerning this clinical site, please contact Nymox at 800-936-9669. Towson Maryland

Sponsors (1)

Lead Sponsor Collaborator
Nymox Corporation

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary American Urological Association Symptom Index (AUASI) 365 days
Secondary American Urological Association Symptom Index (AUASI) 90 days
Secondary American Urological Association Symptom Index (AUASI) 180 days
Secondary American Urological Association Symptom Index (AUASI) 270 days
Secondary Peak urine flow rate (Qmax) 365 days
Secondary Peak urine flow rate (Qmax) 90 days
Secondary Peak urine flow rate (Qmax) 180 days
See also
  Status Clinical Trial Phase
Completed NCT03052049 - Prostatic Artery Embolization (PAE) for Treatment of Signs and Symptoms of Benign Prostatic Hyperplasia (BPH) Using Bead Block Microspheres N/A
Recruiting NCT04757116 - Post-Market Study to Assess iTind Safety in Comparison to UroLift N/A
Completed NCT03460873 - Prognostic Factor in the Patients With Benign Prostatic Hyperplasia Who Undergo Holmium Laser Enucleation of the Prostate
Completed NCT01218243 - An Efficacy Trial of Electroacupuncture at Points of Bilateral BL33 for Mild and Moderate Benign Prostatic Hyperplasia Phase 2
Completed NCT01566292 - Intraprostatic Botulinum Toxin Type "A" Injection in Patients With Benign Prostatic Hyperplasia and Unsatisfactory Response to Medical Therapy Phase 2/Phase 3
Active, not recruiting NCT00407953 - PROLIEVE® Post-Marketing Study TREATMENT OF BENIGN PROSTATIC HYPERPLASIA (BPH) Phase 4
Completed NCT03191734 - French Aquablation Clinical Investigation Using Waterjet Ablation Therapy for Endoscopic Resection of Prostate Tissue N/A
Recruiting NCT04838769 - REZŪM vs. Dual Drug Therapy for Symptomatic Benign Prostatic Hyperplasia in Sexually Active Men N/A
Completed NCT03856242 - Benign Prostatic Hyperplasia and Ischemic Heart DIsease Phase 4
Completed NCT04032067 - Evaluate the Efficacy and Safety of GV1001 in Patients With Benign Prostatic Hyperplasia (BPH) Phase 3
Completed NCT02505919 - Waterjet Ablation Therapy for Endoscopic Resection of Prostate Tissue (WATER) N/A
Completed NCT02855892 - A Phase II Clinical Trial to Evaluate the Efficacy and Safety of GV1001 in Patients With BPH Phase 2
Completed NCT02145208 - Study to Assess the Efficacy of Medi-Tate iTind Device N/A
Completed NCT00970632 - A Study of Tadalafil in Men With Benign Prostatic Hyperplasia Phase 3
Recruiting NCT02592473 - Prostate Artery Embolization (PAE) for Treatment of Benign Prostatic Hyperplasia N/A
Completed NCT00759135 - Phase 2 Study of NX-1207 for the Treatment of Benign Prostatic Hyperplasia (BPH) (Enlarged Prostate) Phase 2
Completed NCT00224107 - A New Drug for Benign Prostatic Hyperplasia (BPH) Compared With Placebo Phase 3
Recruiting NCT04648176 - Application of MOSES Technology in BPH N/A
Terminated NCT00651807 - A Trial to Investigate the Effectiveness and Safety of Org 3236 (Etonogestrel) Tablets in Men With Urinary Complaints Suggestive of a Benign Enlargement of the Prostate (304001)(P05806) Phase 2
Recruiting NCT04766268 - Prostate Artery Embolization: Single Center Experience N/A