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Completed Phase 2 Interventional

Eight-Weeks Of Treatment With Talnetant In Subjects With Irritable Bowel Syndrome (IBS)

ClinicalTrials.gov ID: NCT00101985

Public ClinicalTrials.gov record NCT00101985. 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 17, 2026, 11:35 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

An Eight-week, Randomized, Double-blind, Placebo-controlled, Dose-ranging Study to Evaluate Efficacy and Safety of Talnetant in Subjects With Irritable Bowel Syndrome

Brief summary

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

This study will evaluate the effectiveness and safety of the investigational drug talnetant in treating subjects with irritable bowel syndrome (IBS).

Study identification

NCT ID
NCT00101985
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
741 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
Oct 2004 (Type not available)
Primary completion
Jul 2005 (Actual)
Completion
Jul 2005 (Actual)
Last update posted
Apr 13, 2015

2004 – 2005

United States locations

U.S. sites
70
U.S. states
31
U.S. cities
66
Facility City State ZIP Site status
GSK Investigational Site Chandler Arizona 85224 —
GSK Investigational Site Phoenix Arizona 85016 —
GSK Investigational Site North Little Rock Arkansas 72117 —
GSK Investigational Site Carmichael California 95608 —
GSK Investigational Site Concord California 94520 —
GSK Investigational Site Garden Grove California 92840 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Roseville California 95661 —
GSK Investigational Site Spring Valley California 91978 —
GSK Investigational Site Torrance California 90506 —
GSK Investigational Site Boulder Colorado 80304 —
GSK Investigational Site Centennial Colorado 80112 —
GSK Investigational Site Wheat Ridge Colorado 80033 —
GSK Investigational Site Bristol Connecticut 06010 —
GSK Investigational Site Stamford Connecticut 06905 —
GSK Investigational Site Torrington Connecticut 06790 —
GSK Investigational Site Newark Delaware 19713 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site St. Petersburg Florida 33707 —
GSK Investigational Site St. Petersburg Florida 33709 —
GSK Investigational Site Atlanta Georgia 30328 —
GSK Investigational Site Riverside Illinois 60546 —
GSK Investigational Site Rockford Illinois 61107 —
GSK Investigational Site Indianapolis Indiana 46237 —
GSK Investigational Site Florence Kentucky 41042 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Slidell Louisiana 70458 —
GSK Investigational Site Silver Spring Maryland 20901 —
GSK Investigational Site Boston Massachusetts 02118 —
GSK Investigational Site Salisbury Massachusetts 01952 —
GSK Investigational Site Springfield Massachusetts 01107 —
GSK Investigational Site Chesterfield Michigan 48047 —
GSK Investigational Site Saint Joseph Michigan 49085 —
GSK Investigational Site Chaska Minnesota 55318 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Lincoln Nebraska 68503 —
GSK Investigational Site Omaha Nebraska 68144 —
GSK Investigational Site Blackwood New Jersey 08012 —
GSK Investigational Site East Syracuse New York 13057 —
GSK Investigational Site Fishkill New York 12524 —
GSK Investigational Site Great Neck New York 11021 —
GSK Investigational Site Rochester New York 14607 —
GSK Investigational Site Rochester New York 14609 —
GSK Investigational Site The Bronx New York 10461 —
GSK Investigational Site Greensboro North Carolina 27403 —
GSK Investigational Site Raleigh North Carolina 27612 —
GSK Investigational Site Wilmington North Carolina 28401 —
GSK Investigational Site Wilmington North Carolina 28412 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Akron Ohio 44310 —
GSK Investigational Site Kettering Ohio 45429 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Medford Oregon 97504 —
GSK Investigational Site Portland Oregon 97225 —
GSK Investigational Site Newtown Pennsylvania 18940 —
GSK Investigational Site Pittsburgh Pennsylvania 15224 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Bristol Tennessee 37620 —
GSK Investigational Site Chattanooga Tennessee 37404 —
GSK Investigational Site Memphis Tennessee 38119 —
GSK Investigational Site Memphis Tennessee 38120 —
GSK Investigational Site Austin Texas 78745 —
GSK Investigational Site El Paso Texas 79905 —
GSK Investigational Site San Antonio Texas 78209 —
GSK Investigational Site Ogden Utah 84405 —
GSK Investigational Site Charlottesville Virginia 22911 —
GSK Investigational Site Christiansburg Virginia 24073 —
GSK Investigational Site Lacey Washington 98516 —

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 65 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00101985, 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 13, 2015 · Synced Oct 17, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00101985 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →