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Terminated Phase 3 Interventional Results available

One Year Study of Rifaximin Delayed Release (DR) Tablets in Crohn's Disease

ClinicalTrials.gov ID: NCT02240121

Public ClinicalTrials.gov record NCT02240121. 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 22, 2026, 10:42 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 Double-Blind, Placebo-Controlled, Parallel-Group, Multicenter, Multiregional, One Year Study to Assess the Efficacy and Safety of Twice Daily Oral Rifaximin Delayed Release Tablets for Induction of Clinical Remission With Endoscopic Response at 16 Weeks Followed by Clinical and Endoscopic Remission at 52 Weeks in Subjects With Active Moderate Crohn's Disease

Brief summary

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

The primary objective is to determine the efficacy of rifaximin DR also referred to as Extended Intestinal Release (EIR) tablets vs. placebo for the induction of clinical remission and endoscopic response following 16 weeks of treatment in participants presenting with active moderate Crohn's disease. A key secondary objective is to evaluate clinical and endoscopic remission following an additional 36 weeks of treatment.

Study identification

NCT ID
NCT02240121
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Bausch Health Americas, Inc.
Industry
Enrollment
80 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
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
Aug 21, 2014 (Actual)
Primary completion
Aug 16, 2017 (Actual)
Completion
Aug 16, 2017 (Actual)
Last update posted
Sep 10, 2019

2014 – 2017

United States locations

U.S. sites
72
U.S. states
31
U.S. cities
68
Facility City State ZIP Site status
Not listed Scottsdale Arizona 85260 —
Not listed Tucson Arizona 85712 —
Not listed Tucson Arizona 85724 —
Not listed Little Rock Arkansas 72205 —
Not listed Little Rock Arkansas 72211 —
Not listed North Little Rock Arkansas 72117 —
Not listed Bakersfield California 93301 —
Not listed Los Angeles California 90067 —
Not listed Mission Hills California 91345 —
Not listed Orange California 92868 —
Not listed San Carlos California 94070 —
Not listed Torrance California 90503 —
Not listed Denver Colorado 80045 —
Not listed Bristol Connecticut 06010 —
Not listed Danbury Connecticut 06810 —
Not listed Boynton Beach Florida 33426 —
Not listed Coral Springs Florida 33071 —
Not listed Hialeah Florida 33012 —
Not listed Homestead Florida 33030 —
Not listed Largo Florida 33777 —
Not listed Miami Florida 33165 —
Not listed Orlando Florida 32803 —
Not listed Orlando Florida 32806 —
Not listed Orlando Florida 32825 —
Not listed Plant City Florida 33563 —
Not listed Winter Haven Florida 33880 —
Not listed Winter Park Florida 32789 —
Not listed Atlanta Georgia 30342 —
Not listed Columbus Georgia 31909 —
Not listed Urbana Illinois 61801 —
Not listed Evansville Indiana 47714 —
Not listed Indianapolis Indiana 46202 —
Not listed Pratt Kansas 67124 —
Not listed Madisonville Kentucky 42431 —
Not listed Chevy Chase Maryland 20815 —
Not listed Towson Maryland 21204 —
Not listed Marlborough Massachusetts 01752 —
Not listed Ann Arbor Michigan 48109 —
Not listed Chesterfield Michigan 48047 —
Not listed Troy Michigan 48098 —
Not listed Jackson Mississippi 39202 —
Not listed Mexico Missouri 65265 —
Not listed Reno Nevada 89511 —
Not listed Marlton New Jersey 08053 —
Not listed Teaneck New Jersey 07666 —
Not listed Brooklyn New York 11235 —
Not listed Flushing New York 11355 —
Not listed Great Neck New York 11021 —
Not listed New York New York 10016 —
Not listed Poughkeepsie New York 12601 —
Not listed Chapel Hill North Carolina 27599 —
Not listed Jacksonville North Carolina 28546 —
Not listed Kinston North Carolina 28501 —
Not listed Raleigh North Carolina 27612 —
Not listed Salisbury North Carolina 28144 —
Not listed Mentor Ohio 44060 —
Not listed Oklahoma City Oklahoma 73104 —
Not listed Sayre Pennsylvania 18840 —
Not listed Charleston South Carolina 29406 —
Not listed Greenville South Carolina 29615 —
Not listed Orangeburg South Carolina 29118 —
Not listed Sioux Falls South Dakota 57108 —
Not listed Kingsport Tennessee 37660 —
Not listed Nashville Tennessee 37211 —
Not listed Arlington Texas 76012 —
Not listed Fort Worth Texas 76104 —
Not listed Pasadena Texas 77505 —
Not listed Southlake Texas 76092 —
Not listed Clinton Utah 84015 —
Not listed Leesburg Virginia 20176 —
Not listed Bellevue Washington 98004 —
Not listed Madison Wisconsin 53705-2281 —

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 NCT02240121, 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 Sep 10, 2019 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02240121 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →