Trial Profile

A Randomised, Double-blind, Placebo-controlled, Parallel Group, Dose-titration Study to Determine the Efficacy and Safety of VA106483 in Male Subjects With Nocturia.

Status: Completed

Phase of Trial: Phase II

Latest Information Update: 03 Oct 2021

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At a glance

Drugs Fedovapagon (Primary)
Indications Benign prostatic hyperplasia; Lower urinary tract symptoms; Nocturia
Focus Therapeutic Use
Sponsors Vantia Therapeutics

Most Recent Events

07 Sep 2010 Status changed from active, no longer recruiting to completed as reported by ClinicalTrials.gov.
19 May 2010 Planned end date changed from 1 Jul 2010 to 1 Aug 2010 as reported by ClinicalTrials.gov.
19 May 2010 Status changed from recruiting to active, no longer recruiting as reported by ClinicalTrials.gov.

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