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Completed Phase 2 Interventional

A Phase 2, Multi-center Study to Evaluate the Efficacy and Safety of ONO-2952 in Female Subjects With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)

ClinicalTrials.gov ID: NCT01844180

Public ClinicalTrials.gov record NCT01844180. 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 25, 2026, 8:19 AM 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, Multi-center, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of ONO-2952 in Female Subjects With Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D)

Brief summary

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

The objective of this study is to explore efficacy, safety and tolerability of ONO-2952 in female subjects with Diarrhea-Predominant Irritable Bowel Syndrome (IBS-D).

Study identification

NCT ID
NCT01844180
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Ono Pharma USA Inc
Industry
Enrollment
200 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 65 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
Apr 2013 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Not listed
Last update posted
Apr 15, 2016

Started 2013

United States locations

U.S. sites
48
U.S. states
22
U.S. cities
48
Facility City State ZIP Site status
Anniston Clinical Site Anniston Alabama 36207 —
Goodyear Clinical Site Goodyear Arizona 85351 —
Tucson Clinical Site Tucson Arizona 85712 —
North Little Rock Clinical Site North Little Rock Arkansas 72120 —
Carlsbad Clinical Site Carlsbad California 92008 —
San Diego Clinical Site San Diego California 92114 —
Boynton Beach Clinical Site Boynton Beach Florida 33426 —
Clearwater Clinical Site Clearwater Florida 33756 —
Deland Clinical Site DeLand Florida 32720 —
Hialeah Clinical Site Hialeah Florida 33012 —
Lauderdale Lakes Clinical Site Lauderdale Lakes Florida 33319 —
Orlando Clinical Site Orlando Florida 32806 —
Port Orange Clinical Site Port Orange Florida 32129 —
South Miami Clinical Site South Miami Florida 33143 —
St. Petersburg Clinical Site St. Petersburg Florida 33709 —
Tampa Clinical Site Tampa Florida 33606 —
West Palm Clinical Site West Palm Florida 33409 —
Oak Lawn Clinical Site Oak Lawn Illinois 60453 —
Wichita Clinical Site Wichita Kansas 67203 —
New Orleans Clinical Site New Orleans Louisiana 70115 —
Chesterfield Clincial Site Chesterfield Michigan 48047 —
Billings Clinical Site Billings Montana 59102 —
Reno Clinical Site Reno Nevada 89511 —
Lebanon Clinical Site Lebanon New Hampshire 03756 —
Albuquerque Clinical Site Albuquerque New Mexico 87102 —
Great Neck Clinical Site Great Neck New York 11023 —
Cary Clinical Site Cary North Carolina 27518 —
Highpoint Clinical Site Highpoint North Carolina 27262 —
Raleigh Clinical Site Raleigh North Carolina 27612 —
Winston-Salem Clinical Site Winston-Salem North Carolina 27103 —
Akron Clinical Site Akron Ohio 44311 —
Columbus Clinical Site Columbus Ohio 43212 —
Dayton Clinical Site Dayton Ohio 45432 —
Groveport Clinical Site Groveport Ohio 43125 —
Mentor Clinical Site Mentor Ohio 44060 —
Norman Clinical Site Norman Oklahoma 73069 —
Lansdale Clinical Site Landsdale Pennsylvania 19446 —
Greer Clinical Site Greer South Carolina 29650 —
Mt. Pleasant Clinical Site Mt. Pleasant South Carolina 29464 —
Chattanooga Clinical Site Chattanooga Tennessee 37421 —
Germantown Clinical Site Germantown Tennessee 38138 —
Pasadena Clinical Site Pasadena Texas 77505 —
Plano Clinial Site Plano Texas 75075 —
San Antonio Clinical Site San Antonio Texas 78229 —
Logan Clinical Site Logan Utah 84341 —
Ogden Clinical Site Ogden Utah 84405 —
Salt Lake City Clinical Site Salt Lake City Utah 84107 —
Sandy Clinical Site Sandy City Utah 84094 —

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 NCT01844180, 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 Apr 15, 2016 · Synced Oct 25, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01844180 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →