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NCT02637960 · ClinicalTrials.gov registry record · Phase 2

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

A Phase 2 study, sponsored by Vantia.

Completed
Registry status
Phase 2
Development phase
432
Enrollment target

NCT02637960: Completed Phase 2 study, sponsored by Vantia.

NCT02637960 is a Phase 2 study that has completed, run by Vantia. The registered enrollment target is 432 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (225% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02637960, a Phase 2 study, has completed, sponsored by Vantia.

COMPLETED
Registry status
Phase 2
Development phase
432 participants
Enrollment target

Study Summary

This study will investigate the efficacy and safety of fedovapagon in the treatment of nocturia in men with BPH.

Interventions

  • DRUG Placebo
  • DRUG Fedovapagon 2 mg

Trial Details

FieldValue
Enrollment Target 432 participants
Start Date 2016-03
Est. Completion 2017-08
Phase Phase 2
Vantia

6 total trials

What the finished NCT02637960 record still lists

NCT02637960 is an interventional study that assigns participants to a tested intervention. The registered 432 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (225% higher).

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT02637960 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02637960 about?

NCT02637960 is a clinical study titled "Efficacy Study of Fedovapagon for Nocturia in Men With Benign Prostatic Hyperplasia (BPH)". This study will investigate the efficacy and safety of fedovapagon in the treatment of nocturia in men with BPH.

What is the current status of trial NCT02637960?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 432 participants. The study started on 2016-03. Estimated completion is 2017-08.

What interventions are being tested in trial NCT02637960?

The interventions under investigation include: Placebo (DRUG), Fedovapagon 2 mg (DRUG).

Who is sponsoring clinical trial NCT02637960?

This trial is sponsored by Vantia, which has 6 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02637960's enrollment target sits among peer trials

432 90th of 2000 higher than 1,911 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02637960, the US trial registry maintained by the National Library of Medicine. NCT02637960 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.