Efficacy of Eluxadoline in the Treatment of Irritable Bowel Syndrome With Diarrhea in Patients With Inadequate Control of Symptoms With Prior Loperamide Use

Study Identifier
CMO-US-GI-0429
CT.gov Identifier
EudraCT Identifier
Not available
EUCTIS ID
Not available
For general inquiries, please contact
Study Complete

Results Available

Protocol
Available Language(s): English
Statistical Analysis Plan
Available Language(s): English

Study Details

Medical Condition
  • Irritable Bowel Syndrome (IBS)
  • Study Drug
  • Eluxadoline
  • Placebo
  • Phase
    Phase 4
    Sex
    Female & Male
    Age
    18 - 80 Years

    Protocol Summary

    This study will evaluate the efficacy and safety of eluxadoline 100 milligrams (mg) twice a day (BID) versus placebo for the treatment of patients with Irritable Bowel Syndrome with Diarrhea (IBS-D) who report that the use of loperamide in the prior 12 months failed to provide control of their IBS-D symptoms.

    Study Locations

    Location
    Status
    Location
    Clinical Research Associates, LLC
    Huntsville, Alabama, United States, 35801
    Status
    Not applicable
    Location
    The Center for Clinical Trials
    Saraland, Alabama, United States, 36571
    Status
    Not applicable
    Location
    Elite Clinical Studies
    Phoenix, Arizona, United States, 85018
    Status
    Not applicable
    Location
    Arkansas Gastroenterology
    North Little Rock, Arkansas, United States, 72117
    Status
    Not applicable
    Location
    Med Investigations
    Carmichael, California, United States, 95608
    Status
    Not applicable
    Location
    GW Research Inc
    Chula Vista, California, United States, 91910
    Status
    Not applicable
    Showing {first} - {last} of {total} Results