Nocturia Clinical Trial
Official title:
A Randomised, Double-blind, Placebo-controlled, Multi-centre Study to Investigate the Efficacy and Safety of Fedovapagon in the Treatment of Nocturia in Men With Benign Prostatic Hyperplasia (BPH) (EQUINOC Study)
This study will investigate the efficacy and safety of fedovapagon in the treatment of nocturia in men with BPH.
Fedovapagon is a selective vasopressin V2 receptor (V2R) agonist that has an antidiuretic
effect through stimulation of V2 receptors in the kidney and is being developed for the
treatment of nocturia. Nocturia, defined as the complaint that the individual has to wake at
night one or more times to void, is a common condition and shows an age-dependent increase in
both prevalence and severity (number of nocturnal voids). It has a significant detrimental
impact on the quality of life in patients with benign prostatic hyperplasia (BPH).
The purpose of this study is to determine the efficacy and safety of fedovapagon in the
treatment of nocturia with BPH.
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