A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of Rifaximin 550 mg Tid in the Treatment of Subjects With Non-Constipation Irritable Bowel Syndrome.

Trial Profile

A Phase 3, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Assess the Efficacy and Safety of Rifaximin 550 mg Tid in the Treatment of Subjects With Non-Constipation Irritable Bowel Syndrome.

Completed
Phase of Trial: Phase III

Latest Information Update: 19 Oct 2016

At a glance

  • Drugs Rifaximin (Primary)
  • Indications Irritable bowel syndrome
  • Focus Registrational; Therapeutic Use
  • Acronyms TARGET-2
  • Sponsors Salix Pharmaceuticals
  • Most Recent Events

    • 27 May 2015 According to a media release, Rifaximin (Xifaxan) 550 mg was approved by US FDA for the treatment of IBS-D in adults based on the data from this and two other phase III trials (TARGET-1, CTP 700031240 and TARGET-3; CTP 700204719 ).
    • 22 May 2012 Results of a pooled analysis from his trial (TARGET-2) and TARGET-1 presented at the Digestive Disease Week 2012.
    • 22 May 2012 Pooled quality-of-life analysis presented at Digestive Disease Week 2012.
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