drugset / Trial / NCT03806127

Study to Evaluate the Efficacy and Safety of Vibegron Administered Orally for 12 Weeks to Women With Irritable Bowel Syndrome

NCT03806127

Phase 2 Completed 222 enrolled Urovant Sciences GmbH
RandomizedParallel-groupTriple-blindTreatment

Summary

This study will evaluate the efficacy and safety of vibegron, a beta-3 adrenergic receptor (β3-AR) agonist, in the treatment of pain associated with irritable bowel syndrome (IBS) due to IBS with predominant diarrhea (IBS-D) or mixed episodes of diarrhea and constipation (IBS-M).

Timeline

Start
2018-12-31
Primary completion
2020-09-25
Completion
2020-10-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Vibegron Unknown 75 mg Oral