REVEAL HPS-3 TIMI-55 trial
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Rim Halaby, M.D. [2]
Official Title
REVEAL: Randomized EValuation of the Effects of Anacetrapib Through Lipid-modification. A Large-scale, Randomized Placebo-controlled Trial of the Clinical Effects of Anacetrapib Among People With Established Vascular Disease
Objective
The Randomized EValuation of the Effects of Anacetrapib Through Lipid-modification (REVEAL) trial aims to determine whether lipid modification with anacetrapib 100mg daily reduces the risk of coronary death, myocardial infarction (MI) or coronary revascularization (collectively known as major coronary events) in patients with circulatory problems who have their Low-density Lipoprotein (LDL) cholesterol level treated with a statin.
Sponsor
University of Oxford
Timeline
| Timeline | |
| Start Date | June 2011 |
| End Date | January 2017 |
| Status | This study is ongoing, but not recruiting participants. |
The previous information was derived from ClinicalTrials.gov on 08/18/2014 using the identification number NCT01252953.
Study Description
| Study Description | |
| Study Type | Interventional |
| Study Phase | Phase 3 |
| Study Design | |
| Allocation | Randomized |
| Endpoint | Safety/Efficacy Study |
| Interventional Model | Parallel Assignment |
| Masking | Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor) |
| Study Details | |
| Primary Purpose | Prevention |
| Condition | Atherosclerotic cardiovascular disease |
| Intervention | Drug: anacetrapib Drug: placebo anacetrapib |
| Study Arms |
Experimental: anacetrapib |
| Population Size | 30624 |
The previous information was derived from ClinicalTrials.gov on 09/19/2013 using the identification number NCT01252953.
Eligibility Criteria
Inclusion Criteria
Patients must be aged at least 50 at the time of initial invitation, and at least one of the following inclusion criteria must be satisfied:
- History of MI; or
- Cerebrovascular atherosclerotic disease (i.e. history of presumed ischemic stroke or carotid revascularization); or
- Peripheral arterial disease (i.e. history of non-coronary revascularization, including aortic aneurysm repair or graft); or
- Diabetes mellitus with other evidence of symptomatic coronary heart disease (i.e. treatment or hospitalization for angina, or a history of coronary revascularization or acute coronary syndrome).
Exclusion Criteria
None of the following must be satisfied:
- Acute MI, acute coronary syndrome or stroke within 4 weeks prior to Screening Visit or during Run-in (but such individuals may be entered later, if appropriate)
- Planned coronary revascularization procedure within the next 6 months (such individuals may be entered later, if appropriate)
- Definite history of chronic liver disease, or abnormal liver function (i.e. alanine transaminase (ALT) >2x the upper limit of normal (ULN)). Note: Individuals with a history of acute hepatitis are eligible provided this ALT limit is not exceeded
- Severe renal insufficiency (i.e. creatinine >200 µmol/L [2.3 mg/dL], dialysis or functioning renal transplant)
- Evidence of active inflammatory muscle disease (e.g. dermatomyositis, polymyositis), or creatine kinase (CK) >3x ULN
- Previous significant adverse reaction to a statin or anacetrapib
- Current treatment with any of the following lipid-lowering treatments: (i) a regimen considered to produce substantially greater LDL cholesterol reduction than atorvastatin 80 mg daily for individuals in non-Asian countries or 20 mg daily for those in North East Asia or (ii) fibric acid derivative ("fibrate", including gemfibrozil) or (iii) niacin (nicotinic acid) at doses above 100 mg daily
- Concurrent treatment with a medication that is contraindicated with anacetrapib or atorvastatin:
- Any potent CYP3A4 inhibitor, such as:
- macrolide antibiotics (erythromycin, clarithromycin, telithromycin)
- systemic imidazole or triazole antifungals (e.g. itraconazole, posaconazole)
- protease inhibitors (e.g. atazanavir)
- nefazodone
- ciclosporin
- daptomycin
- systemic use of fusidic acid (Note: Individuals who are taking such drugs temporarily may be re-screened when they discontinue them, if considered appropriate)
- Any potent CYP3A4 inhibitor, such as:
- Known to be poorly compliant with clinic visits or prescribed medication
- Medical history that might limit the individual's ability to take trial treatments for the duration of the study (e.g. severe respiratory disease history of cancer or evidence of spread within last 5 years, other than non-melanoma skin cancer or recent history of alcohol or substance misuse)
- Women of child-bearing potential (unless using adequate contraception)
- Current participation in a clinical trial with an unlicensed drug or device
Individuals will also be excluded at the Screening visit if it is considered unlikely that they will achieve total cholesterol <3.5 mmol/L (135 mg/dL) on the highest atorvastatin dose available in their region (atorvastatin 80 mg daily in non-Asian countries or 20 mg daily in North East Asia).
In addition, individuals will be excluded at the Randomization visit if any of the following are true:
- Total cholesterol above 4 mmol/L [155 mg/dL]
- Non-compliant with run-in treatment (<90% scheduled run-in medication taken)
- Individual is no longer willing to be randomized into the 4-5 year trial
- The individual's doctor is of the view that their patient should not be randomized
Outcomes
Primary Outcomes
The primary outcomes are major coronary events (defined as coronary death, myocardial infarction or coronary revascularization procedure).
Primary assessment will involve an intention-to-treat comparison among all randomized participants of the effects of allocation to anacetrapib versus placebo on major coronary events (defined as the occurrence of coronary death, myocardial infarction or coronary revascularization procedure) during the scheduled treatment period.
Publications
Results
Pending
Conclusion
Pending