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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 Jun 26, 2026, 3:57 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

Study identification

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

Conditions and interventions

Interventions

  • Other: Placebo Drug
  • GSK232802 Drug
  • PREMARIN Drug

Drug

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 16, 2007
Primary completion
Jul 22, 2008
Completion
Jul 22, 2008
Last update posted
Oct 2, 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 2, 2017 · Synced Jun 26, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00604825 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →