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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.
CW ID: 178190
Date Last Changed:
May 2, 2014
Debbie Johnson, CCRC, Director of ResearchFirst Urology, PSC101 Hospital Blvd.Jeffersonville, IN 47130Phone: (812) 206-8161Fax: (812) 288-2612
First Urology, PSC
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