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Completed Phase 3 Interventional

Intravenous And Oral Casopitant (GW679769) For The Prevention Of Chemotherapy Induced Nausea And Vomiting

ClinicalTrials.gov ID: NCT00366834

Public ClinicalTrials.gov record NCT00366834. 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 21, 2026, 1:14 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 III, Multicenter, Randomized, Double-Blind, Active Controlled, Parallel Group Study of the Safety and Efficacy of the Intravenous and Oral Formulations of the Neurokinin-1 Receptor Antagonist Casopitant (GW679769) in Combination With Ondansetron and Dexamethasone for the Prevention of Nausea

Brief summary

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

This is a Phase III trial designed to demonstrate that casopitant (GW679769) plus dexamethasone and ondansetron is more effective in the prevention of vomiting than dexamethasone and ondansetron alone following the administration of moderately emetogenic chemotherapy.

Study identification

NCT ID
NCT00366834
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
1,840 participants

Conditions and interventions

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
Jul 2006 (Type not available)
Primary completion
Oct 2007 (Actual)
Completion
Oct 2009 (Actual)
Last update posted
Sep 10, 2012

2006 – 2009

United States locations

U.S. sites
86
U.S. states
33
U.S. cities
81
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35209 —
GSK Investigational Site Birmingham Alabama 35233 —
GSK Investigational Site Glendale Arizona 85304 —
GSK Investigational Site Fayetteville Arkansas 72703 —
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Jonesboro Arkansas 72401 —
GSK Investigational Site Concord California 94520 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Fresno California 93710 —
GSK Investigational Site Greenbrae California 94904-2007 —
GSK Investigational Site La Verne California 91750 —
GSK Investigational Site Los Angeles California 90057 —
GSK Investigational Site Orange California 92868 —
GSK Investigational Site Poway California 92064 —
GSK Investigational Site San Diego California 92121 —
GSK Investigational Site Soquel California 95073 —
GSK Investigational Site Norwich Connecticut 06360 —
GSK Investigational Site Washington D.C. District of Columbia 20010 —
GSK Investigational Site Boynton Beach Florida 33435 —
GSK Investigational Site Brooksville Florida 34613 —
GSK Investigational Site Fort Lauderdale Florida 33316 —
GSK Investigational Site Fort Lauderdale Florida 33328 —
GSK Investigational Site Inverness Florida 34452 —
GSK Investigational Site Miami Florida 33179 —
GSK Investigational Site New Port Richey Florida 34652 —
GSK Investigational Site Tamarac Florida 33321 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site West Palm Beach Florida 33401 —
GSK Investigational Site Augusta Georgia 30912 —
GSK Investigational Site Columbus Georgia 31904 —
GSK Investigational Site Lawrenceville Georgia 30045 —
GSK Investigational Site Centralia Illinois 62801 —
GSK Investigational Site Galesburg Illinois 61401 —
GSK Investigational Site Skokie Illinois 60076 —
GSK Investigational Site Evansville Indiana 47713 —
GSK Investigational Site Muncie Indiana 47303 —
GSK Investigational Site Terre Haute Indiana 47804 —
GSK Investigational Site Mason City Iowa 50401 —
GSK Investigational Site Hazard Kentucky 41701 —
GSK Investigational Site Lexington Kentucky 40503 —
GSK Investigational Site Alexandria Louisiana 71301 —
GSK Investigational Site Baton Rouge Louisiana 70809 —
GSK Investigational Site Metairie Louisiana 70006 —
GSK Investigational Site Baltimore Maryland 21229-5299 —
GSK Investigational Site Baltimore Maryland 21237 —
GSK Investigational Site Pittsfield Massachusetts 01201 —
GSK Investigational Site Worcester Massachusetts 01608 —
GSK Investigational Site Clinton Township Michigan 48038 —
GSK Investigational Site Free Soil Michigan 49411 —
GSK Investigational Site Saint Joseph Michigan 49085 —
GSK Investigational Site Troy Michigan 48085 —
GSK Investigational Site Hattiesburg Mississippi 39401 —
GSK Investigational Site Tupelo Mississippi 38801 —
GSK Investigational Site Jefferson City Missouri 65109 —
GSK Investigational Site Rolla Missouri 65401 —
GSK Investigational Site St Louis Missouri 63141 —
GSK Investigational Site Billings Montana 59101 —
GSK Investigational Site Great Falls Montana 59405 —
GSK Investigational Site Denville New Jersey 07834 —
GSK Investigational Site Newark New Jersey 07112 —
GSK Investigational Site Somerville New Jersey 08876 —
GSK Investigational Site Sparta New Jersey 07871 —
GSK Investigational Site Albuquerque New Mexico 87109 —
GSK Investigational Site Buffalo New York 14215 —
GSK Investigational Site Durham North Carolina 27710 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Bismarck North Dakota 58501 —
GSK Investigational Site Akron Ohio 44304 —
GSK Investigational Site Bethlehem Pennsylvania 18015 —
GSK Investigational Site Hershey Pennsylvania 17033 —
GSK Investigational Site Sayre Pennsylvania 18840 —
GSK Investigational Site Mt. Pleasant South Carolina 29464 —
GSK Investigational Site Sumter South Carolina 29150 —
GSK Investigational Site Corpus Christi Texas 78412 —
GSK Investigational Site Corpus Christi Texas 78463-3069 —
GSK Investigational Site Dallas Texas 75237 —
GSK Investigational Site Richardson Texas 75080 —
GSK Investigational Site Logan Utah 84341 —
GSK Investigational Site Ogden Utah 84403 —
GSK Investigational Site Burlington Vermont 05401 —
GSK Investigational Site Everett Washington 98201 —
GSK Investigational Site Spokane Washington 99204 —
GSK Investigational Site Tacoma Washington 98405 —
GSK Investigational Site Huntington West Virginia 25701 —
GSK Investigational Site Huntington West Virginia 25705 —
GSK Investigational Site Madison Wisconsin 53717 —

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 137 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00366834, 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, 2012 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00366834 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →