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

Completed · Phase 2 · Has a placebo group

Conditions studied: Irritable Bowel Syndrome (IBS)

In brief

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

Key facts

Study ID

NCT00421707

Run by

GlaxoSmithKline

People needed

133

Starts

2006-10-14

Expected to finish

2008-06-25

Last updated by the study team

2018-01-31

Who can join

Age: 18 and older, up to 64. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• The subject has been diagnosed with IBS consistent with the Rome II Criteria as adapted in Appendix 3 of the protocol
• The subject has normal results from a flexible sigmoidoscopy, colonoscopy, or a flexible sigmoidoscopy plus barium enema, according to subject's age, within 5 years of randomization. Otherwise, the appropriate procedure(s) must be performed and normal results obtained during the 7-day procedure window (prior to randomization):
• If the subject is < 50 years of age and has not had a colonic examination within 5 years of the Screening Visit, flexible sigmoidoscopy, or colonoscopy must be performed.
• If the subject is = 50 years of age and has not had a colonic examination within 5 years of the Screening Visit, a colonoscopy or flexible sigmoidoscopy plus barium enema must be performed.
• Colonic procedure results must be known prior to randomization into the study and dispensing study medication
• During the two-week screening phase, the subject must have conducted self assessments on = 10 days of 14 day (with 80% compliance on daily IVRS calls) compliance assessment using the telephone data entry system

You may not qualify if…

• As a result of any of the medical interview, physical examination, evaluation of mental state and psychiatric history or screening investigations the physician
• Subject reported no stool for 7 consecutive days during the two-week screening phase responsible considers the subject unfit for the study
• The subject has a concurrent illness or disability that may affect the interpretation of clinical data, or otherwise contraindicates participation in this clinical study (e.g., an unstable cardiovascular, autoimmune, renal, hepatic, pulmonary, endocrine, metabolic, gastrointestinal, haematological, or neurological condition).

Where it is running

• GSK Investigational Site — Sherwood, Arkansas, United States
• GSK Investigational Site — Concord, California, United States
• GSK Investigational Site — Los Angeles, California, United States
• GSK Investigational Site — Tampa, Florida, United States
• GSK Investigational Site — Stockbridge, Georgia, United States
• GSK Investigational Site — Louisville, Kentucky, United States
• GSK Investigational Site — Monroe, Louisiana, United States
• GSK Investigational Site — Boston, Massachusetts, United States
• GSK Investigational Site — St Louis, Missouri, United States
• GSK Investigational Site — Greensboro, North Carolina, United States
• GSK Investigational Site — Anderson, South Carolina, United States
• GSK Investigational Site — Greer, South Carolina, United States
• GSK Investigational Site — Chattanooga, Tennessee, United States
• GSK Investigational Site — Germantown, Tennessee, United States
• GSK Investigational Site — Austin, Texas, United States
• GSK Investigational Site — San Antonio, Texas, United States
• GSK Investigational Site — Lynchburg, Virginia, United States
• GSK Investigational Site — Truro, Nova Scotia, Canada
• GSK Investigational Site — Toronto, Ontario, Canada
• GSK Investigational Site — Toronto, Ontario, Canada
• GSK Investigational Site — Toronto, Ontario, Canada
• GSK Investigational Site — Toronto, Ontario, Canada
• GSK Investigational Site — Saskatoon, Saskatchewan, Canada

Full record on ClinicalTrials.gov

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