A Study to Evaluate Daily Pravastatin, Fenofibrate or Pravafen in the Treatment of Combined Hyperlipidemia

Completed · Phase 3

Conditions studied: Combined Hyperlipidemia

In brief

This is a multi-center, double blind, prospective, longitudinal, randomized, 12-week study with a 52-week open-label follow-up to evaluate the safety and efficacy of daily administration of Pravastatin 40 mg or Fenofibrate 160 mg or Pravafen (the combination of both Pravastatin and Fenofibrate 40/160 mg) in the treatment of combined hyperlipidemia. There will be an open-label, 8-week, Selection Phase prior to randomization in which all patients will be stabilized on Pravastatin 40 mg/day. Following the Selection Phase, and if the patients meet all inclusion/exclusion criteria, they will be randomized to a three arm, double blind, 12-week Efficacy Phase during which they would receive either Pravastatin 40 mg or Fenofibrate 160 mg or Pravafen (the combination of Pravastatin and Fenofibrate 40/160 mg). The 12-week Efficacy Phase will be followed by an open-label, 52-week, Safety Phase in which all patients will receive Pravafen. After the 8-week Selection Phase, patients that still meet the inclusion/exclusion criteria will be randomized on a 1:1:2 ratio to Pravastatin 40 mg or Fenofibrate 160 mg or Pravafen (the combination of both Pravastatin and Fenofibrate 40/160 mg) for 12 weeks. After the completion of the 12-week double-blind phase of the study, all patients that haven't had changes in their well being, will be allowed to roll-over into the 52-week, open-label, follow-up portion of the study. During the 52 week, open label, Safety Phase of the study, all patients will receive Pravafen (the combination of Pravastatin and Fenofibrate 40/160 mg). Patients will be evaluated at baseline and every three weeks thereafter throughout the initial 12-week Efficacy Phase of the study. Patients that roll-over into the 52-week, open-label, follow-up Safety Phase will be evaluated at 12, 24, 36 and 52 weeks. Participation in the study can be up to 72 weeks.

Key facts

Study ID

NCT00459745

Run by

Shionogi

People needed

481

Starts

2007-04-01

Expected to finish

2009-07-01

Last updated by the study team

2018-04-24

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Patients meeting all the criteria listed below may be selected to enroll into the Selection Phase of the study:
• Male or female patients from 18-75 years of age, inclusive at the time of dosing with a history of a combined hyperlipidemia.
• High LDL cholesterol and TG levels as per the table hereunder:
• Prior treatment LDL Cholesterol TG Naïve to treatment* > 130 mg/dL and ≥ 150 mg/dL and ≤ 400 mg/dL Lipid Lowering Monotherapy > 130 mg/dL and ≥ 150 mg/dL and ≤ 400 mg/dL Lipid Lowering Combination Therapy > 110 mg/dL and ≥ 150 mg/dL and ≤ 400 mg/dL
• A patient that has received NO lipid lowering therapy within 6 weeks prior to the Selection Visit, will be considered Naïve to treatment.
• If the patient is female and of childbearing potential and sexually active, an acceptable birth control method must be used (abstinence, IUD, oral, transdermal, injectable or implantable contraceptives, at least 2 years post-menopausal, one year post hysterectomy, double barrier device and/or partner at least one year post vasectomy), a negative serum pregnancy test must be obtained at the Selection Visit (Visit 1) and a negative urine pregnancy test must be obtained prior to study drug administration at Baseline Visit (Visit 3).
• Able to comply with all study procedures.
• Patients that provide a written informed consent to participate in the study indicated by a personal signature and date on the patient consent form.
• At the end of the Selection Phase, patients meeting all of the criteria listed below may be selected and randomized into the Efficacy Phase of the study:
• Selected patients with LDL Cholesterol ≥ 100 mg/dl and/or TG ≥ 150 mg/dl and ≤ 400 mg/dl at Week-1 / Visit 2 after taking Pravastatin 40 mg/day from Visit 1.
• Patients still meeting the selection criteria a, c, d and e as listed under section 4.1.
• Patients with a compliance ≥ 80% during the 8-week Pravastatin phase of the study.

You may not qualify if…

• Patients will be excluded from the study if any one or more of the following apply:
• Female of childbearing potential who is pregnant and/or lactating and/or sexually active but not using an acceptable method of contraception
• History of allergy or contraindications to:
• fenofibrate or similar compounds
• HMG-CoA reductase inhibitors
• History of uncontrolled or unstable;
• diabetes ((i.e., diabetic nephropathy etc.),
• hepatic impairment/insufficiency,
• renal impairment/insufficiency (i.e., nephritis, polycystic kidney disease, acute or chronic renal failure, end-stage renal disease, GFR < 60 ml/min, etc.),
• neurological,
• gastrointestinal (ulcerative colitis, Barrett's, etc.),
• gallbladder disease (patients with prior cholecystectomy can be allowed to participate),
• psychiatric disease,
• sleep apnea
• any other clinically significant medical or surgical history that could affect the safety of the patient or hinder the evaluation of drug effect based on Investigator or Medical Monitor discretion
• Acute liver disease or persistent elevations in liver function tests (2 times the upper normal limit or greater)
• Levels of creatine phosphokinase (CK) 3 times the upper normal limit or greater
• Change in diuretic or β-blocker treatment for hypertension within 30 days of enrollment into the selection phase (Visit 1)
• Positive personal history of abuse of any of the following:
• Alcohol (as per the DSM-IV criteria) and/or
• Recreational drugs (as per the DSM-IV criteria)
• Usage of any of the following medications (patients must have discontinued these medications for 5 or more half-lives or for 30 days, whichever is greater prior to study drug administration on Visit 3 / Day 0) :
• Corticosteroids
• Immunosuppressants
• Macrolide antibiotics

Where it is running

• Cochise Clinical Research — Sierra Vista, Arizona, United States
• Memorial Research Medical Clinic — Long Beach, California, United States
• Clinical Trials Research — Roseville, California, United States
• Orange County Research Center — Tustin, California, United States
• Jacksonville Center for Clinical Research — Jacksonville, Florida, United States
• Jacksonville Center for Clinical Research — Jacksonville, Florida, United States
• Drug Study Institute — Jupiter, Florida, United States
• Mima Century Research Associates — Melbourne, Florida, United States
• Cardiology Research Associates — Ormond Beach, Florida, United States
• Atlanta Vascular Research Foundation — Atlanta, Georgia, United States
• East-West Medical Research Institute — Honolulu, Hawaii, United States
• Welborn Clinic Research Center — Evansville, Indiana, United States
• MediSphere Medical Research Center LLC — Evansville, Indiana, United States
• Research Institute of Middle America — Jeffersonville, Indiana, United States
• Welborn Clinic Gateway — Newburgh, Indiana, United States
• Lemarc Research Center — Louisville, Kentucky, United States
• Bluegrass Clinical Research, Inc. — Louisville, Kentucky, United States
• Androscoggin Cardiology Associates — Auburn, Maine, United States
• MODEL Clinical Research — Baltimore, Maryland, United States
• Health Trends Research, LLC — Baltimore, Maryland, United States
• MD Medical Research — Oxon Hill, Maryland, United States
• Clinical Research Center of Cape Cod, Inc — West Yarmouth, Massachusetts, United States
• Clinical Study Site — Florissant, Missouri, United States
• Mercy Medical Group — Manchester, Missouri, United States
• Anasazi Internal Medicine — Phoenix, Arizona, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.