A Randomized, Double-blind, Placebo-controlled Dose-ranging Study of OPK-88004 Once-a-day Dosing for 16 Weeks in Men With Signs and Symptoms of Benign Prostatic Hyperplasia. NCT03297398, SAR-202

  • STATUS
    Not Recruiting
Updated on 29 September 2022

Summary

This study will evaluate the safety and effectiveness of different doses of OPK-88004 compared to placebo on prostate size and related lower urinary tract symptoms (LUTS) in men with benign prostatic hyperplasia (BPH).

Description

For more information contact Cheryl Zinar, Director of Clinical Research, Urologic Consultants of Southeastern PA.

Details
Condition Benign Prostatic Hyperplasia (Enlarged Prostate)
Clinical Study IdentifierTX196750
Last Modified on29 September 2022

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