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Clinical trial

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)

NCT02637960 is registered in ClinicalTrials.gov with Vantia Ltd as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

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)
Lead sponsor
Vantia Ltd
Phase
Phase 2/3
Overall status
Completed
Start date
March 31, 2016
Completion date
August 31, 2017
Enrollment
432 (actual)
Sites
48

Conditions

As the registry lists them; a condition with its own page is linked.