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.