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A Study in People With Abnormal Fat Levels in the Blood

Phase 2
Completed
Conditions
Dyslipidemia
Registration Number
NCT00116519
Lead Sponsor
Eli Lilly and Company
Brief Summary

The purposes of this study are to determine:

* The safety of the study medication and any side effects that might be associated with it;

* Whether the study medication can help patients with low levels of 'good' cholesterol (HDL-C) and high blood fats or triglycerides (TG);

* How much of the study medication should be given to patients;

* How the study medication compares to fenofibrate (Lofibra), a drug used for people with low levels of HDL-C and high levels of TG.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
300
Inclusion Criteria
  • Men and women between 18 and 80 years of age
  • People with abnormal fat levels in the blood (low HDL, high TG)
Exclusion Criteria
  • People with diabetes
  • People whose blood pressure is greater than 160/95 mm Hg, on or off blood pressure medicine
  • People who have had frequent chest pain or unstable angina, a heart attack or a heart procedure, including stent placement, within the past 3 months

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Primary Outcome Measures
NameTimeMethod
Effects on HDL-C and Triglycerides after 12 weeks
Safety after 12 weeks
Secondary Outcome Measures
NameTimeMethod
Effects on factors of metabolic syndrome after 12 weeks
Effects on biomarkers of atherosclerosis after 12 weeks
Effects on LDL-C after 12 weeks

Trial Locations

Locations (1)

For additional information regarding investigative sites for this trial, contact 1-877-CTLILLY (1-877-285-4559, 1-317-615-4559) Mon - Fri from 9 AM to 5 PM Eastern Time (UTC/GMT - 5 hours, EST), or speak with your personal physician. test

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Wenatchee, Washington, United States

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