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Completed Phase 2 Interventional

A Study To Evaluate An NK-1 Antiemetic For The Prevention Of Post Operative Nausea And Vomiting

ClinicalTrials.gov ID: NCT00108095

Public ClinicalTrials.gov record NCT00108095. 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, 7:08 AM 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 Multicenter, Randomized, Double-blind, Placebo-controlled, Dose-ranging, Parallel Group Phase II Study to Evaluate the Safety, Efficacy and Pharmacokinetics of the Oral Neurokinin-1 Receptor Antagonist, GW679769, When Administered With Intravenous Ondansetron Hydrochloride for the Prevention of Post-operative Nausea and Vomiting (PONV) and Post-discharge Nausea and Vomiting (PDNV) in Female Subjects With Known Risk Factors for PONV Who Are Undergoing Surgical Procedures Associated With an Increased Emetogenic Risk

Brief summary

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

This study is looking at a range of doses of this NK-1 receptor antagonist drug, for both safety and effectiveness in prevention PONV

Study identification

NCT ID
NCT00108095
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
701 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 55 Years
Sex
Female
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
Aug 2005 (Actual)
Completion
Aug 2005 (Actual)
Last update posted
Jan 20, 2017

2004 – 2005

United States locations

U.S. sites
30
U.S. states
17
U.S. cities
27
Facility City State ZIP Site status
GSK Investigational Site Montgomery Alabama 36106 —
GSK Investigational Site Phoenix Arizona 85032 —
GSK Investigational Site Arcadia California 91007 —
GSK Investigational Site Duarte California 91010 —
GSK Investigational Site Glendale California 91206 —
GSK Investigational Site Laguna Hills California 92653 —
GSK Investigational Site Loma Linda California 92354 —
GSK Investigational Site Pasadena California 91109 —
GSK Investigational Site San Diego California 92123 —
GSK Investigational Site Stanford California 94305 —
GSK Investigational Site Naples Florida 34108 —
GSK Investigational Site Pensacola Florida 32504 —
GSK Investigational Site Alpharetta Georgia 30005 —
GSK Investigational Site Hutchinson Kansas 67502 —
GSK Investigational Site Kansas City Kansas 66160 —
GSK Investigational Site Baton Rouge Louisiana 70806 —
GSK Investigational Site Baltimore Maryland 21229-5299 —
GSK Investigational Site Jackson Mississippi 39202 —
GSK Investigational Site New Brunswick New Jersey 8903 —
GSK Investigational Site New York New York 10016 —
GSK Investigational Site New York New York 10025 —
GSK Investigational Site Winston-Salem North Carolina 27103 —
GSK Investigational Site Pittsburgh Pennsylvania 15213 —
GSK Investigational Site Charleston South Carolina 29425 —
GSK Investigational Site Houston Texas 77024 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Houston Texas 77054 —
GSK Investigational Site San Antonio Texas 78240 —
GSK Investigational Site Winchester Virginia 22601 —
GSK Investigational Site Wenatchee Washington 98801 —

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 28 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00108095, 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 20, 2017 · 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 NCT00108095 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →