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Completed Phase 2 Interventional Results available

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

ClinicalTrials.gov ID: NCT03806127

Public ClinicalTrials.gov record NCT03806127. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 2:00 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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).

Study identification

NCT ID
NCT03806127
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Urovant Sciences GmbH
Industry
Enrollment
222 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 70 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 31, 2018 (Actual)
Primary completion
Sep 25, 2020 (Actual)
Completion
Oct 6, 2020 (Actual)
Last update posted
Aug 2, 2021

2018 – 2020

United States locations

U.S. sites
41
U.S. states
18
U.S. cities
38
Facility City State ZIP Site status
Synexus Clinical Research US, Inc.-Simon Williamson Clinic Birmingham Alabama 35211 —
Clinical Research Associates Huntsville Alabama 35801 —
Alabama Medical Group, PC Mobile Alabama 36693 —
Hope Research Institute Chandler Arizona 85224 —
Synexus Clinical Research US, Inc. - East Valley Family Physicians, PLC Chandler Arizona 85224 —
Synexus Clinical Research US, Inc. - Central Arizona Medical Associates, PC Mesa Arizona 85206 —
Synexus Clinical Research US, Inc. - Desert Clinical Research, LLC Mesa Arizona 85213 —
Synexus - Clinical Research Advantage, Inc. - Central Phoenix Medical Clinic LLC Phoenix Arizona 85020 —
GW Research Inc - ClinEdge-PPDS Chula Vista California 91910 —
Triwest Research Associates, LLC La Mesa California 91942 —
VA Long Beach Healthcare System - NAVREF Long Beach California 90822 —
Southern California Research Institute Medical Group, Inc. Los Angeles California 90045 —
Desta Digestive Disease Medical Center San Diego California 92114 —
Medical Associates Research Group, Inc. San Diego California 92123 —
Torrance Clinical Research Torrance California 90505 —
Medical Research Center of Connecticut LLC Hamden Connecticut 06518 —
Mayo Clinic - Division of Gastroenterology Jacksonville Florida 32224 —
Florida Center For Gastroenterology Largo Florida 33777 —
Clinical Research Center of Florida Pompano Beach Florida 33060 —
Palm Beach Research - ClinEdge - PPDS West Palm Beach Florida 33409 —
RNA America, LLC Sugar Hill Georgia 30518 —
Investigators Research Group, LLC Indianapolis Indiana 46268 —
Mandeville Private Physician Group, LLC Mandeville Louisiana 70471 —
Massachusetts General Hospital Boston Massachusetts 02114 —
University of Michigan Ann Arbor Michigan 48109 —
Clinical Research Institute of Michigan Chesterfield Michigan 48047 —
Synexus Clinical Research US, Inc. - Rita B. Chuang, MD, LLC Henderson Nevada 89502 —
Advanced Research Institute Reno Nevada 89511 —
Atrium Healthcare Center for Digestive Health Charlotte North Carolina 28204 —
Carolina Digestive Diseases Greenville North Carolina 27834 —
East Carolina Gastroenterology Jacksonville North Carolina 28546 —
Dayton Gastroenterology, Inc. Beavercreek Ohio 45440 —
Central Sooner Research Norman Oklahoma 73071 —
Synexus Clinical Research US, Inc. - Anderson Anderson South Carolina 29621 —
Chattanooga Medical Research Inc Chattanooga Tennessee 37404 —
Clinical Research Solutions PC Jackson Tennessee 38305 —
DHAT Research Institute Garland Texas 75044 —
University of Texas Health Science Center at Houston Houston Texas 77030 —
Synexus Clinical Research US, Inc.-Plano Plano Texas 75093 —
Synexus Clinical Research US, Inc. - Wasatch Peak Family Practice Layton Utah 84041 —
Advanced Research Institute South Ogden Utah 84405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03806127, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2021 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT03806127 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →