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Therapeutic Areas: Nephrology | Urology | Family Medicine
Disease Category: Benign Prostatic Hyperplasia (Enlarged Prostate)
Location: United States, IN
A Phase III multi-center prospective randomized, parallel-group, placebo-controlled, double-blind, clinical evaluation of NX-1207 for the treatment of BPH (Benign Prostatic Hyperplasia, or Enlarged Prostate)
The purpose of this study is to evaluate the efficacy and safety of NX-1207 and to see if it could be useful for men with BPH. The study treatment will consist of either an injection of NX-1207 or of a placebo into the prostate. If you end up receiving the placebo, you will be offered the chance to receive NX-1207 at the end of the study. The study will last for 12 months.
- Male ≥ 45 years of age
- History of BPH for at least 1 year
- Acute or chronic Prostatitis in the past 12 months
- Urinary Tract Infections more than once in the past 12 months
- Previous surgical or invasive prostate treatments such as TURP, TUMT, and TUNA, laser or any minimally invasive treatments.
- History of urinary retention in the past 12 months
- Prostate or bladder cancer
- PSA ≥ 10 ng.ml
Debbie Johnson, CCRC, Director of Research
First Urology, PSC. (formerly Metropolitan Urology and Allied Urology)
101 Hospital Blvd.
Jeffersonville, IN 47130
Phone: (812) 206-8161
Fax: (812) 288-2612
If you would like to learn more about participating in this study, please send an email message using the form below.
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