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Completed Phase 2 Interventional

Dyslipidemia Study Investigating The Increase In "Good Cholesterol"

ClinicalTrials.gov ID: NCT00169559

Public ClinicalTrials.gov record NCT00169559. 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 22, 2026, 4:54 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 Multi-center, Three-staged, Randomized, Parallel Group, Sequential, Double-blind, fenofibrate-and Placebo-controlled Dose-response Evaluation of the Safety, Tolerability, and Effects on Plasma HDLc and TG of Eight Weeks Treatment With 1µg to 20µg Daily Doses of GW590735 in Otherwise Healthy Subjects With Low HDLc, Mildly to Moderately Elevated TG, and Normal LDLc

Study identification

NCT ID
NCT00169559
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
GlaxoSmithKline
Industry
Enrollment
250 participants

Conditions and interventions

Conditions

Interventions

  • GW590735 Drug
  • fenofibrate 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
Oct 31, 2003
Primary completion
Mar 31, 2005
Completion
Mar 31, 2005
Last update posted
Oct 21, 2012

2003 – 2005

United States locations

U.S. sites
45
U.S. states
20
U.S. cities
41
Facility City State ZIP Site status
GSK Investigational Site Birmingham Alabama 35243
GSK Investigational Site Phoenix Arizona 85014
GSK Investigational Site Phoenix Arizona 85050
GSK Investigational Site Scottsdale Arizona 85251
GSK Investigational Site Beverly Hills California 90210
GSK Investigational Site Healdsburg California 95448
GSK Investigational Site Orange California 92868
GSK Investigational Site Spring Valley California 91978
GSK Investigational Site Walnut Creek California 94598
GSK Investigational Site DeLand Florida 32720
GSK Investigational Site Fort Lauderale Florida 33308
GSK Investigational Site Fort Lauderdale Florida 33145
GSK Investigational Site Fort Lauderdale Florida 33308
GSK Investigational Site Hollywood Florida 33021
GSK Investigational Site Jacksonville Florida 32205
GSK Investigational Site Jacksonville Florida 32216
GSK Investigational Site Pembroke Pines Florida 33024
GSK Investigational Site Orland Park Illinois 60462
GSK Investigational Site Evansville Indiana 47714
GSK Investigational Site Indianapolis Indiana 46260
GSK Investigational Site Iowa City Iowa 52242
GSK Investigational Site Louisville Kentucky 40213
GSK Investigational Site Auburn Maine 04210
GSK Investigational Site Brooklyn Center Minnesota 55430
GSK Investigational Site Omaha Nebraska 68131
GSK Investigational Site Endwell New York 13760
GSK Investigational Site New York New York 10021
GSK Investigational Site Rochester New York 14609
GSK Investigational Site Williamsville New York 14221
GSK Investigational Site Statesville North Carolina 28677
GSK Investigational Site Wilmington North Carolina 28412
GSK Investigational Site Cincinnati Ohio 45219
GSK Investigational Site Cincinnati Ohio 45246
GSK Investigational Site Medford Oregon 97504
GSK Investigational Site Allentown Pennsylvania 18102
GSK Investigational Site Erie Pennsylvania 16506
GSK Investigational Site Sioux Falls South Dakota 57105
GSK Investigational Site Bristol Tennessee 37620
GSK Investigational Site Kingsport Tennessee 37660
GSK Investigational Site Bryan Texas 77802
GSK Investigational Site Conroe Texas 77304
GSK Investigational Site Houston Texas 77030
GSK Investigational Site San Antonio Texas 78229
GSK Investigational Site Norfolk Virginia 23502
GSK Investigational Site Richmond Virginia 23294

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00169559, 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 21, 2012 · Synced Jul 22, 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 NCT00169559 live on ClinicalTrials.gov.

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