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Completed Phase 3 Interventional

Prevention of Seasonal Affective Disorder

ClinicalTrials.gov ID: NCT00046449

Public ClinicalTrials.gov record NCT00046449. 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 Jul 23, 2026, 5:35 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Study identification

NCT ID
NCT00046449
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
Not listed

Conditions and interventions

Interventions

  • Investigational Seasonal Affective Disorder (SAD) Drug Drug

Drug

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
Aug 31, 2002
Primary completion
May 31, 2003
Completion
May 31, 2003
Last update posted
Jun 3, 2015

2002 – 2003

United States locations

U.S. sites
47
U.S. states
19
U.S. cities
42
Facility City State ZIP Site status
Study Site Homer Alaska 99603
Study Site New Haven Connecticut 06504-0605
Study Site Newark Delaware 19713
Study Site Wilmington Delaware 19808-1251
Study Site Washington D.C. District of Columbia 20016
Study Site Washington D.C. District of Columbia 20037
Study Site Boise Idaho 83704
Study SIte Chicago Illinois 60610
Study Site Chicago Illinois 60612
Study Site Hoffman Estates Illinois 60194
Study Site Libertyville Illinois 60048
Study SIte Northfield Illinois 60093
Study Site Schaumburg Illinois 60194
Study SIte Greenwood Indiana 46143
Study Site Indianapolis Indiana 45202
Study Site Florence Kentucky 41042
Study Site Wellesley Hills Massachusetts 02481
Study Site Okemos Michigan 48864
Study Site Royal Oak Michigan 48067
Study Site Minneapolis Minnesota 55454
Study Site Moorestown New Jersey 08057
Study Site Piscataway New Jersey 08854
Study Site Amityville New York 11701
Study Site Lawrence New York 11559
Study Site New York New York 10021
Study Site Olean New York 14760
Study Site Staten Island New York 10305
Study Site Williamsville New York 14221
Study Site Cincinnati Ohio 45219
Study Site Cleveland Ohio 44106
Study Site Cleveland Ohio 44121
Study Site Independence Ohio 44131
Study Site Lyndhurst Ohio 44124
Study Site Toledo Ohio 43623
Study Site Eugene Oregon 97401
Study Site Portland Oregon 97201
Study Site Portland Oregon 97209
Study Site Salem Oregon 97309
Study Site Allentown Pennsylvania 18104
Study Site Philadelphia Pennsylvania 19106
Study Site Philadelphia Pennsylvania 19107
Study Site Lincoln Rhode Island 02865-4208
Study Site Seattle Washington 98104
Study Site Madison Wisconsin 53719
Study Site Middleton Wisconsin 53562
Study Site Milwaukee Wisconsin 53226
Study Site West Allis Wisconsin 53227

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00046449, 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 Jun 3, 2015 · Synced Jul 23, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00046449 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →