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Last Updated: February 24, 2020

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CLINICAL TRIALS PROFILE FOR FENOFIBRATE

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All Clinical Trials for Fenofibrate

Trial ID Title Status Sponsor Phase Start Date Summary
NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Completed Centers for Disease Control and Prevention Phase 3 1999-09-01 The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Completed National Eye Institute (NEI) Phase 3 1999-09-01 The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Completed National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK) Phase 3 1999-09-01 The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Completed National Institute on Aging (NIA) Phase 3 1999-09-01 The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
NCT00000620 Action to Control Cardiovascular Risk in Diabetes (ACCORD) Completed National Heart, Lung, and Blood Institute (NHLBI) Phase 3 1999-09-01 The purpose of this study is to prevent major cardiovascular events (heart attack, stroke, or cardiovascular death) in adults with type 2 diabetes mellitus using intensive glycemic control, intensive blood pressure control, and multiple lipid management.
NCT00006412 Safety and Effectiveness of Fenofibrate and Pravastatin in HIV-Positive Patients With Abnormal Blood Lipids Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 3 1969-12-31 The purpose of this study is to compare the safety and effectiveness of fenofibrate and pravastatin in treating HIV-positive patients who have abnormal levels of fat (lipids) in the blood. Increased lipids in the blood associated with HIV infection and anti-HIV drugs is a growing problem. The drugs used in this study are known to reduce certain lipids, but little is known about their safety and effectiveness. This study will see if one of the drugs is safer and more effective than the other, or if combining the drugs is the safest and most effective way to lower lipids. This study has been changed. On June 26, 2001, this study was reviewed by the Data and Safety Monitoring Board (DSMB). The DSMB is an independent board monitoring the progress of the study. The review showed that neither pravastatin nor fenofibrate alone were effective in reaching all the cholesterol and triglyceride goals. There were no safety concerns. It is not known if the combination of fenofibrate and pravastatin is effective and safe. Therefore, it is important to continue this study.
NCT00076518 The Effect of Fish Oil Plus Fenofibrate on Triglyceride Levels in People Taking Highly Active Antiretroviral Therapy (HAART) Completed National Institute of Allergy and Infectious Diseases (NIAID) Phase 2 1969-12-31 The purpose of this study is to determine the effectiveness of fish oil supplements combined with the drug fenofibrate in treating elevated triglyceride levels in people taking anti-HIV drugs. The participants in this study will have shown no response to fish oil supplements or fenofibrate alone.
>Trial ID >Title >Status >Phase >Start Date >Summary

Clinical Trial Conditions for Fenofibrate

Condition Name

Condition Name for Fenofibrate
Intervention Trials
Dyslipidemia 23
Hypertriglyceridemia 19
Hyperlipidemia 15
Healthy 9
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Condition MeSH

Condition MeSH for Fenofibrate
Intervention Trials
Dyslipidemias 40
Hyperlipidemias 27
Hypertriglyceridemia 24
Diabetes Mellitus, Type 2 14
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Clinical Trial Locations for Fenofibrate

Trials by Country

Trials by Country for Fenofibrate
Location Trials
United States 320
Canada 22
Germany 15
India 13
Korea, Republic of 13
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Trials by US State

Trials by US State for Fenofibrate
Location Trials
Florida 20
California 18
Texas 17
Illinois 16
Ohio 15
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Clinical Trial Progress for Fenofibrate

Clinical Trial Phase

Clinical Trial Phase for Fenofibrate
Clinical Trial Phase Trials
Phase 4 34
Phase 3 38
Phase 2/Phase 3 7
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Clinical Trial Status

Clinical Trial Status for Fenofibrate
Clinical Trial Phase Trials
Completed 94
Recruiting 17
Terminated 14
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Clinical Trial Sponsors for Fenofibrate

Sponsor Name

Sponsor Name for Fenofibrate
Sponsor Trials
Solvay Pharmaceuticals 17
Abbott 10
Merck Sharp & Dohme Corp. 8
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Sponsor Type

Sponsor Type for Fenofibrate
Sponsor Trials
Other 101
Industry 95
NIH 20
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