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A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome

Trial Profile

A Phase 2, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 19 Dec 2022

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At a glance

  • Drugs Vibegron (Primary)
  • Indications Abdominal pain
  • Focus Proof of concept; Therapeutic Use
  • Sponsors Urovant Sciences
  • Most Recent Events

    • 01 Dec 2022 Results assessing the efficacy and safety of the beta3 -adrenergic agonist vibegron in treating irritable bowel syndrome related pain published in the Neurogastroenterology and Motility
    • 25 Nov 2020 Status changed from active, no longer recruiting to completed.
    • 24 Nov 2020 According to a Urovant Sciences Media Release, the company will continue to analyze the full data set of this study.

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