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Clinical Trial Details — Status: Terminated

Administrative data

NCT number NCT02227784
Other study ID # 14502
Secondary ID I1V-MC-EIBH
Status Terminated
Phase Phase 3
First received
Last updated
Start date October 2014
Est. completion date December 2015

Study information

Verified date September 2019
Source Eli Lilly and Company
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The purpose of the ACCENTUATE study is to evaluate whether the study drug known as evacetrapib is effective in treating participants with high cholesterol and atherosclerotic cardiovascular disease (ASCVD) and/or diabetes.


Recruitment information / eligibility

Status Terminated
Enrollment 366
Est. completion date December 2015
Est. primary completion date December 2015
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Must be treated with atorvastatin 40 mg/day for at least 30 days prior to screening

- Have an LDL-C >70 mg/deciliter(dL) or non-HDL-C >100 mg/dL

- Have screening triglycerides =400 mg/dL (=4.5 millimoles/Liter)

- Individuals with ASCVD and/or individuals with type 1 or type 2 diabetes

Exclusion Criteria:

- Have a hemoglobin A1c (HbA1c) >9.5%

- New York Heart Association (NYHA) class III or IV congestive heart failure

- History of either a transient ischemic stroke or ischemic stroke <30 days

- History of acute coronary syndrome (ACS) <30 days

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Evacetrapib
Administered orally
Atorvastatin
Administered orally
Ezetimibe
Administered orally
Placebo
Administered orally

Locations

Country Name City State
Puerto Rico Research and Cardiovascular Corp. Ponce
Puerto Rico Clinical Research Puerto Rico, Inc. San Juan
Puerto Rico GCM Medical Group PSC San Juan
United States Northwest Heart Clinical Research, LLC Arlington Heights Illinois
United States Asheville Cardiology Associates Asheville North Carolina
United States University of Colorado Health Sciences Center Aurora Colorado
United States Maryland Cardiovascular Specialists Baltimore Maryland
United States Overlea Personal Physicians Baltimore Maryland
United States Northwest Clinical Research Center Bellevue Washington
United States Grace Research Bossier City Louisiana
United States ZASA Clinical Research Boynton Beach Florida
United States Advanced Clinical Research Carmichael California
United States Metrolina Internal Medicine, P.A. Charlotte North Carolina
United States Cedar-Crosse Research Center Chicago Illinois
United States Cardiac Research Colorado Springs Colorado
United States Aventiv Research Columbus Ohio
United States Georgia Heart Specialists Covington Georgia
United States Midwest CRC Crystal Lake Illinois
United States Partners in Clinical Research Cumberland Rhode Island
United States Cardiology Research Assoc. Daytona Beach Florida
United States Avail Clinical Research LLC DeLand Florida
United States Tooraj Joseph Raoof M.D., Inc. Encino California
United States Lillestol Research LLC Fargo North Dakota
United States Alan Graff, MD, PA Fort Lauderdale Florida
United States United Osteoporosis Center Gainesville Georgia
United States High Point Clinical Trials Center High Point North Carolina
United States East West Medical Institute Honolulu Hawaii
United States Heart Center Research, LLC Huntsville Alabama
United States Hutchinson Clinic Hutchinson Kansas
United States Cape Cod Research Institute Hyannis Massachusetts
United States Indiana Heart Physicians Inc Indianapolis Indiana
United States Midwest Institute for Clinical Research Indianapolis Indiana
United States Nature Coast Clinical Research, LLC Inverness Florida
United States Irvine Clinical Research Center Irvine California
United States Clinical Investigation Specialists Inc Kenosha Wisconsin
United States Holston Medical Group Clinical Research Kingsport Tennessee
United States Palm Research Center Las Vegas Nevada
United States VA Long Beach Healthcare System Long Beach California
United States Community Medical Associates Louisville Kentucky
United States Solaris Clinical Research Meridian Idaho
United States Desert Clinical Research Mesa Arizona
United States ActivMed Practices & Research, Inc Methuen Massachusetts
United States Suncoast Research Group, LLC Miami Florida
United States PMG Research of Charleston, LLC Mount Pleasant South Carolina
United States Medex Healthcare Research, Inc. New York New York
United States South Oklahoma Heart Research, LLC Oklahoma City Oklahoma
United States Central Phoenix Med Clinic LLC Phoenix Arizona
United States Progressive Medical Research Port Orange Florida
United States Portland Preventive Cardiology, LLC Portland Oregon
United States Rancho Cucamonga Clinical Rancho Cucamonga California
United States Black Hills Cardiovascular Research Group Rapid City South Dakota
United States National Clinical Research - Richmond Richmond Virginia
United States Boice Willis Clinic, PA Rocky Mount North Carolina
United States Medex Healthcare Research, Inc. Saint Louis Missouri
United States Saratoga Clinical Research LLC Saratoga Springs New York
United States Heart and Vascular Center of New Brunswick LLC Somerset New Jersey
United States Kootenai Heart Clinics, LLC Spokane Washington
United States Encompass Clinical Research Spring Valley California
United States Northwest Houston Heart Center Tomball Texas
United States University Clinical Investigators, Inc. Tustin California
United States Diablo Clinical Research Walnut Creek California
United States Cardiology Partners Clinical Research Institute, LLC Wellington Florida
United States Buffalo Cardiology and Pulmonary Associates, P.C. Williamsville New York
United States PMG Research of Wilmington, LLC Wilmington North Carolina

Sponsors (1)

Lead Sponsor Collaborator
Eli Lilly and Company

Countries where clinical trial is conducted

United States,  Puerto Rico, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change From Baseline to 3 Months in Low-Density Lipoprotein Cholesterol (LDL-C) Change in LDL-C levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. LDL-C was measured by beta quantification. Statistics are from analysis of covariance with log baseline measurement and treatment is included in the model. Least Square Means (LS means) and median differences were analyzed in log units and converted to standard units. Log Percent change from baseline response is the dependent variable. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in High-Density Lipoprotein Cholesterol (HDL-C) Change in HDL-C levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. LS medians and median differences were analyzed in log units and converted to standard units. Statistics are from mixed model repeated measures analysis with log baseline measurement, treatment, visit, and treatment by visit interaction included in the model. Log percent change from baseline response is the dependent variable. Within-participant repeated measures at multiple visits are modeled by a compound symmetry covariance structure. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in Apolipoprotein AI (apoAI) Change in apoAI levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. Statistics are from analysis of covariance with log baseline measurement and treatment is included in the model. LS means and median differences were analyzed in log units and converted to standard units. Log Percent change from baseline response is the dependent variable. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in Non-HDL-C Change in Non-HDL-C levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. LS medians and median differences were analyzed in log units and converted to standard units. Statistics are from mixed model repeated measures analysis with log baseline measurement, treatment, visit, and treatment by visit interaction included in the model. Log percent change from baseline response is the dependent variable. Within-participant repeated measures at multiple visits are modeled by a compound symmetry covariance structure. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in Apolipoprotein B (apoB) Change in apoB levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. Statistics are from analysis of covariance with log baseline measurement and treatment is included in the model. LS means and median differences were analyzed in log units and converted to standard units. Log Percent change from baseline response is the dependent variable. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in Cholesterol Efflux Capacity Change in cholesterol efflux capacity from baseline to the 3-month visit expressed as a percentage of the baseline levels. Statistics are from analysis of covariance with log baseline measurement and treatment is included in the model. LS means and median differences were analyzed in log units and converted to standard units. Log Percent change from baseline response is the dependent variable. Baseline, 3 Months
Secondary Percent Change From Baseline to 3 Months in Lipoprotein(a) (Lp[a]) Change in Lp(a) levels from baseline to the 3-month visit expressed as a percentage of the baseline levels. Statistics are from analysis of covariance with log baseline measurement and treatment is included in the model. LS means and median differences were analyzed in log units and converted to standard units. Log Percent change from baseline response is the dependent variable. Baseline, 3 Months
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