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Completed Phase 2Phase 3 Interventional

Efficacy Study of Fedovapagon for Nocturia in Men With Benign Prostatic Hyperplasia (BPH)

ClinicalTrials.gov ID: NCT02637960

Public ClinicalTrials.gov record NCT02637960. 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 Jul 22, 2026, 4:34 AM 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, 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)

Study identification

NCT ID
NCT02637960
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Vantia Ltd
Industry
Enrollment
432 participants

Conditions and interventions

Conditions

Interventions

  • Fedovapagon 2 mg Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 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
Feb 29, 2016
Primary completion
Jun 30, 2017
Completion
Jul 31, 2017
Last update posted
Oct 30, 2018

2016 – 2017

United States locations

U.S. sites
48
U.S. states
20
U.S. cities
48
Facility City State ZIP Site status
Vantia Investigative Center Anniston Alabama
Vantia Investigative Center Goodyear Arizona
Vantia Investigative Center Lincoln California
Vantia Investigative Center Murrieta California
Vantia Investigative Center San Diego California
Vantia Investigative Center Aventura Florida
Vantia Investigative Center Bradenton Florida
Vantia Investigative Center Clearwater Florida
Vantia Investigative Center Coral Gables Florida
Vantia Investigative Center DeLand Florida
Vantia Investigative Center Hialeah Florida
Vantia Investigative Center Miami Florida
Vantia Investigative Center Ocala Florida
Vantia Investigative Center Pembroke Pines Florida
Vantia Investigative Center St. Petersburg Florida
Vantia Investigative Center Tampa Florida
Vantia Investigative Center Avon Indiana
Vantia Investigative Center Topeka Kansas
Vantia Investigative Center Wichita Kansas
Vantia Investigative Center Greenbelt Maryland
Vantia Investigative Center Missoula Montana
Vantia Investigative Center Omaha Nebraska
Vantia Investigative Center Englewood New Jersey
Vantia Investigative Center Lawrenceville New Jersey
Vantia Investigative Center Albuquerque New Mexico
Vantia Investigative Center Garden City New York
Vantia Investigative Center New York New York
Vantia Investigative Center Newburgh New York
Vantia Investigative Center Poughkeepsie New York
Vantia Investigative Center Cary North Carolina
Vantia Investigative Center Concord North Carolina
Vantia Investigative Center High Point North Carolina
Vantia Investigative Center Raleigh North Carolina
Vantia Investigative Center Wilmington North Carolina
Vantia Investigative Center Winston-Salem North Carolina
Vantia Investigative Center Akron Ohio
Vantia Investigative Center Warwick Rhode Island
Vantia Investigative Center Charleston South Carolina
Vantia Investigative Center Greer South Carolina
Vantia Investigative Center Mt. Pleasant South Carolina
Vantia Investigative Center Bristol Tennessee
Vantia Investigative Center Dallas Texas
Vantia Investigative Center Houston Texas
Vantia Investigative Center San Antonio Texas
Vantia Investigative Center Clinton Utah
Vantia Investigative Center Ogden Utah
Vantia Investigative Center Salt Lake City Utah
Vantia Investigative Center Richmond Virginia

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 NCT02637960, 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 Oct 30, 2018 · Synced Jul 22, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02637960 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →