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Completed Phase 2 Interventional

Effects Of GW679769 On Sleep Onset And Maintenance And Next Day Functioning In Subjects With Primary Insomnia

ClinicalTrials.gov ID: NCT00280423

Public ClinicalTrials.gov record NCT00280423. 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, 5:42 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 28 Day, Polysomnographic and Subjective Assessment of GW679769 for the Treatment of Primary Insomnia: A Randomized, Double-blind, Parallel-Group, Placebo-Controlled Trial.

Brief summary

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

This study is designed to find the optimal (best) doses of GW679769 that could be given daily to promote sleep onset and maintain sleep during the night without significant next-day thinking impairment and drowsiness in subjects with primary insomnia.

Study identification

NCT ID
NCT00280423
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
342 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 64 Years
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
Jan 2006 (Type not available)
Primary completion
Feb 2007 (Actual)
Completion
Feb 2007 (Actual)
Last update posted
Apr 15, 2015

2006 – 2007

United States locations

U.S. sites
61
U.S. states
26
U.S. cities
53
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35213 —
GSK Investigational Site Phoenix Arizona 85050 —
GSK Investigational Site Tucson Arizona 85712 —
GSK Investigational Site Little Rock Arkansas 72205 —
GSK Investigational Site Burbank California 91506 —
GSK Investigational Site Huntington Beach California 92648 —
GSK Investigational Site Irvine California 92618 —
GSK Investigational Site Los Angeles California 90048 —
GSK Investigational Site National City California 91950 —
GSK Investigational Site San Diego California 92121 —
GSK Investigational Site San Diego California 92123 —
GSK Investigational Site San Diego California 92161 —
GSK Investigational Site San Francisco California 94105 —
GSK Investigational Site Santa Rosa California 95405 —
GSK Investigational Site Norwalk Connecticut 06850 —
GSK Investigational Site DeLand Florida 32720 —
GSK Investigational Site Delray Beach Florida 33484 —
GSK Investigational Site Hallandale Florida 33009 —
GSK Investigational Site Largo Florida 33773 —
GSK Investigational Site Miami Florida 33143 —
GSK Investigational Site Miami Florida 33173 —
GSK Investigational Site Miami Florida 33176 —
GSK Investigational Site Pembroke Pines Florida 33026 —
GSK Investigational Site Atlanta Georgia 30328 —
GSK Investigational Site Atlanta Georgia 30342 —
GSK Investigational Site Gainesville Georgia 30501 —
GSK Investigational Site Hinesville Georgia 31313 —
GSK Investigational Site Macon Georgia 31201 —
GSK Investigational Site Stockbridge Georgia 30281 —
GSK Investigational Site Chicago Illinois 60611 —
GSK Investigational Site Chicago Illinois 60612 —
GSK Investigational Site Chicago Illinois 60634 —
GSK Investigational Site Overland Park Kansas 66211 —
GSK Investigational Site Crestview Hills Kentucky 41017 —
GSK Investigational Site Rockville Maryland 20852 —
GSK Investigational Site Newton Massachusetts 02459 —
GSK Investigational Site Troy Michigan 48085 —
GSK Investigational Site Hattiesburg Mississippi 39404 —
GSK Investigational Site Las Vegas Nevada 89104 —
GSK Investigational Site Clementon New Jersey 08021 —
GSK Investigational Site West Seneca New York 14224 —
GSK Investigational Site Durham North Carolina 27705 —
GSK Investigational Site Salisbury North Carolina 28144 —
GSK Investigational Site Winston-Salem North Carolina 27157 —
GSK Investigational Site Beachwood Ohio 44122 —
GSK Investigational Site Cincinnati Ohio 45227 —
GSK Investigational Site Cincinnati Ohio 45246 —
GSK Investigational Site Cleveland Ohio 44130 —
GSK Investigational Site Gallipolis Ohio 45631 —
GSK Investigational Site Oklahoma City Oklahoma 73112 —
GSK Investigational Site Gresham Oregon 97020 —
GSK Investigational Site Clarks Summit Pennsylvania 18411 —
GSK Investigational Site Duncansville Pennsylvania 16635 —
GSK Investigational Site Warwick Rhode Island 02886 —
GSK Investigational Site Columbia South Carolina 29201 —
GSK Investigational Site Austin Texas 78756 —
GSK Investigational Site Bellaire Texas 77401 —
GSK Investigational Site Dallas Texas 75251 —
GSK Investigational Site Houston Texas 77030 —
GSK Investigational Site Plano Texas 75093 —
GSK Investigational Site Salt Lake City Utah 84107 —

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 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00280423, 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 Apr 15, 2015 · 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 NCT00280423 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →