Dyslipidemia Study Investigating The Increase In "Good Cholesterol"

Condition(s) targeted: Dyslipidemia; Hypertriglyceridemia

Intervention: GW590735 (Drug); fenofibrate (Drug)

Phase: Phase 2

Status: Completed

Sponsored by: GlaxoSmithKline

Official(s) and/or principal investigator(s):
GSK Clinical Trials, MD, Study Director, Affiliation: GlaxoSmithKline

An eight week comparison of the investigational drug GW590735, placebo, and the marketed drug fenofibrate intended to increase the levels of "good cholesterol" and decrease levels of "bad cholesterol" in healthy patients with low levels of good cholesterol and high levels of bad cholesterol.

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 design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Safety/Efficacy Study

Primary outcome: change from baseline in fasting plasma HDLc concentration at the end of eight weeks of double blind treatment

Secondary outcome: changes from baseline in: fasting plasma total cholesterol, TG, LDLc, ApoA1, ApoA2, Lipoprotein containing ApoA1 and not ApoA2, Lipoprotein containing both ApoA1 and ApoA2, Apo B100, Apo CIII, Free Fatty Acid, insulin, fibrinogen, and C-reactive protein

Minimum age: 18 Years. Maximum age: N/A. Gender(s): Both.

Criteria:

Inclusion criteria:

- High-density lipoprotein cholesterol less than or equal to 45 mg/dL.

- Triglycerides greater than or equal to 120 mg/dL and less than or equal to 500 mg/dL.

- Women must be surgically sterile or postmenopausal.

Exclusion criteria:

- Heart disease

- Diabetes

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Starting date: November 2004
Last updated: September 12, 2005