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Completed Phase 3 Interventional Results available

A Study Of IV Casopitant For The Prevention Of Chemotherapy Induced Nausea And Vomiting.

ClinicalTrials.gov ID: NCT00601172

Public ClinicalTrials.gov record NCT00601172. 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 23, 2026, 1:48 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 Study of Single Dose Intravenous Casopitant in Combination With Ondansetron and Dexamethasone for the Prevention of Oxaliplatin Induced Nausea and Vomiting.

Brief summary

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

This a Phase III trial designed to determine if IV casopitant plus dexamethasone and ondansetron is more effective in the prevention of vomiting and nausea then dexamethasone and ondansetrone alone following the administration of moderately emetogenic oxaliplatin-based chemotherapy.

Study identification

NCT ID
NCT00601172
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
710 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
Mar 10, 2008 (Actual)
Primary completion
Apr 13, 2009 (Actual)
Completion
Apr 13, 2009 (Actual)
Last update posted
Jan 17, 2018

2008 – 2009

United States locations

U.S. sites
23
U.S. states
14
U.S. cities
22
Facility City State ZIP Site status
GSK Investigational Site Hot Springs Arkansas 71913 —
GSK Investigational Site Corona California 92879 —
GSK Investigational Site Fountain Valley California 92708 —
GSK Investigational Site Riverside California 92501 —
GSK Investigational Site St. Petersburg Florida 33705 —
GSK Investigational Site Tampa Florida 33614 —
GSK Investigational Site Alexandria Louisiana 71301 —
GSK Investigational Site Baton Rouge Louisiana 70809 —
GSK Investigational Site Baltimore Maryland 21215-5271 —
GSK Investigational Site Boston Massachusetts 02135 —
GSK Investigational Site Worcester Massachusetts 01608 —
GSK Investigational Site Jefferson City Missouri 65109 —
GSK Investigational Site Great Falls Montana 59405 —
GSK Investigational Site The Bronx New York 10467 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Hilton Head Island South Carolina 29926 —
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 Duncanville Texas 75137 —
GSK Investigational Site Ogden Utah 84403 —
GSK Investigational Site Burlington Vermont 05401 —

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 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00601172, 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 17, 2018 · Synced Oct 23, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00601172 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →