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An Eight-Week, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate Efficacy and Safety of Talnetant in Subjects With Irritable Bowel Syndrome.

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Trial Profile

An Eight-Week, Randomized, Double-Blind, Placebo-Controlled, Dose-Ranging Study to Evaluate Efficacy and Safety of Talnetant in Subjects With Irritable Bowel Syndrome.

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 06 Sep 2023

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At a glance

  • Drugs Talnetant (Primary)
  • Indications Irritable bowel syndrome
  • Focus Therapeutic Use
  • Sponsors GlaxoSmithKline; GSK

    • Most Recent Events

    • 30 Mar 2010 Additional locations [Netherlands] identified as reported by ClinicalTrials.gov.
    • 20 May 2009 Additional locations identified as reported by ClinicalTrials.gov.
    • 15 Oct 2008 Actual start date changed from Oct 2005 to Oct 2004 as reported by Clinicaltrials.gov.

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