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Completed Phase 2 Interventional

Dose Range Finding Study of Fedovapagon in Men With Nocturia

ClinicalTrials.gov ID: NCT01656239

Public ClinicalTrials.gov record NCT01656239. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 24, 2026, 6:03 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double-Blind, Placebo-Controlled, Parallel Group, Dose Range Finding Study To Determine The Efficacy And Safety Of Fedovapagon In Men With Nocturia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to determine the dose level(s) of fedovapagon which result in a decrease in the mean nocturnal void frequency.

Study identification

NCT ID
NCT01656239
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Vantia Ltd
Industry
Enrollment
358 participants

Conditions and interventions

Eligibility (public fields only)

Age range
55 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 2012 (Type not available)
Primary completion
Aug 2013 (Actual)
Completion
Sep 2013 (Actual)
Last update posted
Jun 20, 2014

2012 – 2013

United States locations

U.S. sites
56
U.S. states
30
U.S. cities
56
Facility City State ZIP Site status
Vantia Investigative Center Birmingham Alabama — —
Vantia Investigative Center Huntsville Alabama — —
Vantia Investigative Center Mobile Alabama — —
Vantia Investigative Center Glendale Arizona — —
Vantia Investigative Center Tucson Arizona — —
Vantia Investigative Center Anaheim California — —
Vantia Investigative Center Long Beach California — —
Vantia Investigative Center San Diego California — —
Vantia Investigative Center Denver Colorado — —
Vantia Investigative Center Englewood Colorado — —
Vantia Investigative Center Milford Connecticut — —
Vantia Investigative Center Aventura Florida — —
Vantia Investigative Center Clearwater Florida — —
Vantia Investigative Center Daytona Beach Florida — —
Vantia Investigative Center DeLand Florida — —
Vantia Investigative Center Naples Florida — —
Vantia Investigative Center Ocala Florida — —
Vantia Investigative Center St. Petersburg Florida — —
Vantia Investigative Center Tampa Florida — —
Vantia Investigative Center Coeur d'Alene Idaho — —
Vantia Investigative Center Meridian Idaho — —
Vantia Investigative Center Chicago Illinois — —
Vantia Investigative Center Evansville Indiana — —
Vantia Investigative Center Jeffersonville Indiana — —
Vantia Investigative Center Paducah Kentucky — —
Vantia Investigative Center Metairie Louisiana — —
Vantia Investigative Center Greenbelt Maryland — —
Vantia Investigative Center Rochester Michigan — —
Vantia Investigative Center Edina Minnesota — —
Vantia Investigative Center Omaha Nebraska — —
Vantia Investigative Center Brick New Jersey — —
Vantia Investigative Center Englewood New Jersey — —
Vantia Investigative Center Lawrenceville New Jersey — —
Vantia Investigative Center Albuquerque New Mexico — —
Vantia Investigative Center Brooklyn New York — —
Vantia Investigative Center Endwell New York — —
Vantia Investigative Center Garden City New York — —
Vantia Investigative Center New York New York — —
Vantia Investigative Center Poughkeepsie New York — —
Vantia Investigative Center Concord North Carolina — —
Vantia Investigative Center Raleigh North Carolina — —
Vantia Investigative Center Winston-Salem North Carolina — —
Vantia Investigative Center Cincinnati Ohio — —
Vantia Investigative Center Bethany Oklahoma — —
Vantia Investigative Center Bala-Cynwyd Pennsylvania — —
Vantia Investigative Center Warwick Rhode Island — —
Vantia Investigative Center Mytrle Beach South Carolina — —
Vantia Investigative Center Dakota Dunes South Dakota — —
Vantia Investigative Center Nashville Tennessee — —
Vantia Investigative Center Dallas Texas — —
Vantia Investigative Center Fort Worth Texas — —
Vantia Investigative Center San Antonio Texas — —
Vantia Investigative Center Richmond Virginia — —
Vantia Investigative Center Virginia Beach Virginia — —
Vantia Investigative Center Burien Washington — —
Vantia Investigative Center Middleton Wisconsin — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01656239, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 20, 2014 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01656239 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →