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Completed Phase 2 Interventional Results available

Treatment Of Hot Flashes/Flushes In Postmenopausal Women (WARM Study)

ClinicalTrials.gov ID: NCT00604825

Public ClinicalTrials.gov record NCT00604825. 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 19, 2026, 4:24 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 Parallel-group, Double-blind, Randomized, Placebo-controlled, Active Comparator, Multicenter Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of Two Doses of GSK232802 Administered Orally as Monotherapy for 12 Weeks in Healthy Postmenopausal Women With Moderate to Extremely Severe Vasomotor Symptoms

Brief summary

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

The purpose of this study is to determine whether GSK232802 is safe and effective in reducing the frequency and severity of hot flashes associated with menopause.

Study identification

NCT ID
NCT00604825
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
356 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years to 65 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
Jul 17, 2007 (Actual)
Primary completion
Jul 23, 2008 (Actual)
Completion
Jul 23, 2008 (Actual)
Last update posted
Oct 3, 2017

2007 – 2008

United States locations

U.S. sites
41
U.S. states
22
U.S. cities
38
Facility City State ZIP Site status
GSK Investigational Site Chandler Arizona 85225 —
GSK Investigational Site Glendale Arizona 85308 —
GSK Investigational Site Scottsdale Arizona 85251 —
GSK Investigational Site Tucson Arizona 85710 —
GSK Investigational Site Poway California 92064 —
GSK Investigational Site San Diego California 92103 —
GSK Investigational Site San Diego California 92108 —
GSK Investigational Site Aurora Colorado 80012 —
GSK Investigational Site Boulder Colorado 80301 —
GSK Investigational Site Denver Colorado 80202 —
GSK Investigational Site Wheat Ridge Colorado 80043 —
GSK Investigational Site Washington D.C. District of Columbia 20036 —
GSK Investigational Site Crystal River Florida 34429 —
GSK Investigational Site Fort Myers Florida 33916 —
GSK Investigational Site Jacksonville Florida 32259 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site Pinellas Park Florida 33781 —
GSK Investigational Site Atlanta Georgia 30328 —
GSK Investigational Site Savannah Georgia 31405 —
GSK Investigational Site Overland Park Kansas 66202 —
GSK Investigational Site Louisville Kentucky 40291 —
GSK Investigational Site Sunset Louisiana 70584 —
GSK Investigational Site Saint Clair Shores Michigan 48081 —
GSK Investigational Site Billings Montana 59102 —
GSK Investigational Site Las Vegas Nevada 89119 —
GSK Investigational Site Las Vegas Nevada 89146 —
GSK Investigational Site New Brunswick New Jersey 08901 —
GSK Investigational Site Albuquerque New Mexico 87102 —
GSK Investigational Site Albuquerque New Mexico 87106 —
GSK Investigational Site Chapel Hill North Carolina 27599-7570 —
GSK Investigational Site Cincinnati Ohio 45249 —
GSK Investigational Site Cleveland Ohio 44122 —
GSK Investigational Site Eugene Oregon 97401 —
GSK Investigational Site Portland Oregon 97205 —
GSK Investigational Site Philadelphia Pennsylvania 19114 —
GSK Investigational Site Hilton Head Island South Carolina 29926 —
GSK Investigational Site Dallas Texas 75234 —
GSK Investigational Site Midland Texas 79707 —
GSK Investigational Site Norfolk Virginia 23507 —
GSK Investigational Site Seattle Washington 98105 —
GSK Investigational Site Tacoma Washington 98405 —

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 46 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00604825, 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 Oct 3, 2017 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00604825 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →