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A Double-blind, Placebo-controlled Dose Response Study to Investigate Pharmacodynamics and Pharmacokinetics of Single and Repeated Oral Doses of VA106483 in Elderly Male Subjects

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Trial Profile

A Double-blind, Placebo-controlled Dose Response Study to Investigate Pharmacodynamics and Pharmacokinetics of Single and Repeated Oral Doses of VA106483 in Elderly Male Subjects

Status: Completed
Phase of Trial: Phase I/II

Latest Information Update: 19 Jun 2018

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At a glance

  • Drugs Fedovapagon (Primary)
  • Indications Nocturia
  • Focus Pharmacodynamics; Pharmacokinetics
  • Sponsors Vantia Therapeutics

    • Most Recent Events

    • 21 Jul 2012 Actual end date (2 Feb 2009) added as reported by European Clinical Trials Database record.
    • 21 Jul 2012 New source identified and integrated (European Clinical Trials Database record; EudraCT2008-003774-17).
    • 21 Jul 2012 Primary endpoints added as reported by European Clinical Trials Database record.

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