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Completed Phase 2 Interventional Results available

Randomized Placebo Controlled Efficacy And Safety Study Investigating GW876008 In Patients With Irritable Bowel Syndrome

ClinicalTrials.gov ID: NCT00421707

Public ClinicalTrials.gov record NCT00421707. 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 29, 2026, 10:51 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 PoC in IBS Patients With the CRF1 Receptor Anatgonist, GSK876008

Brief summary

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

This is a double-blind, placebo-controlled, randomised crossover study to investigate the efficacy and safety of GW876008

Study identification

NCT ID
NCT00421707
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
133 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years to 64 Years
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 14, 2006 (Actual)
Primary completion
Jun 25, 2008 (Actual)
Completion
Jun 25, 2008 (Actual)
Last update posted
Jan 31, 2018

2006 – 2008

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
17
Facility City State ZIP Site status
GSK Investigational Site Sherwood Arkansas 72120 —
GSK Investigational Site Concord California 94520 —
GSK Investigational Site Los Angeles California 90095 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Louisville Kentucky 40202 —
GSK Investigational Site Monroe Louisiana 71201 —
GSK Investigational Site Boston Massachusetts 02215 —
GSK Investigational Site St Louis Missouri 63110 —
GSK Investigational Site Greensboro North Carolina 27408 —
GSK Investigational Site Anderson South Carolina 29621 —
GSK Investigational Site Greer South Carolina 29651 —
GSK Investigational Site Chattanooga Tennessee 37404 —
GSK Investigational Site Germantown Tennessee 38138 —
GSK Investigational Site Austin Texas 78705 —
GSK Investigational Site San Antonio Texas 78209 —
GSK Investigational Site Lynchburg Virginia 24502 —

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 6 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00421707, 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 Jan 31, 2018 · Synced Oct 29, 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 NCT00421707 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →