drugset / Trial / NCT01330927

Dose Response Study of VA106483 in Males With Nocturia and Benign Prostatic Hypertrophy (BPH)

NCT01330927 ↗

Phase 1 Completed 30 enrolled Vantia Ltd
RandomizedCrossoverTriple-blindTreatment

Summary

The purpose of this study is to establish the dose response relationship of VA106483 and nocturnal urine volumes in a population of elderly male subjects with Benign Prostatic Hypertrophy (BPH) who are likely to present with nocturia.

Timeline

Start
2011-03
Primary completion
2011-07
Completion
2011-07

Drugs

EvaluationDrugModalityDoseRoute
Subject VA106483 Small molecule 0.5 mg Oral
Subject VA106483 Small molecule 1 mg Oral
Subject VA106483 Small molecule 2 mg Oral
Subject VA106483 Small molecule 4 mg Oral