drugset / Trial / NCT01656239

Dose Range Finding Study of Fedovapagon in Men With Nocturia

NCT01656239 ↗

Phase 2 Completed 358 enrolled Vantia Ltd
RandomizedParallel-groupTriple-blindTreatment

Summary

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.

Timeline

Start
2012-08
Primary completion
2013-08
Completion
2013-09

Drugs

EvaluationDrugModalityDoseRoute
Subject Fedovapagon Unknown 1 mg Oral
Subject Fedovapagon Unknown 2 mg Oral
Subject Fedovapagon Unknown 4 mg Oral

Indications

No indication recorded.