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| ID | Type | Description | Link |
|---|---|---|---|
| 2012-002434-37 | EudraCT Number |
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This study will evaluate the safety and effect of anacetrapib on low-density lipoprotein-cholesterol (LDL-C) when added to ongoing lipid-lowering therapy. The primary hypothesis is that treatment with anacetrapib 100 mg for 12 weeks will lower LDL-C to a greater extent than treatment with placebo.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Anacetrapib | Experimental | Participants receive anacetrapib 100 mg orally once daily for 12 weeks. |
|
| Placebo | Placebo Comparator | Participants receive placebo orally once daily for 12 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Anacetrapib | Drug | 100 mg tablet orally, once daily for 12 weeks |
|
| Measure | Description | Time Frame |
|---|---|---|
| Percent change from Baseline in Low-density Lipoprotein-Cholesterol (LDL-C) using beta-quantification method | Baseline and Week 12 | |
| Number of Participants with Alanine Transaminase (ALT) or Aspartate Aminotransferase (AST) Consecutive Elevations ≥3x Upper Limit of Normal (ULN) | 12 weeks | |
| Number of Participants with Creatine Phosphokinase Elevations ≥10xULN with or without Muscle Symptoms | 12 weeks | |
| Number of Participants with Sodium, Chloride, or Bicarbonate Elevations >ULN or Potassium Levels <Lower Limit of Normal (LLN) | 12 weeks | |
| Number of Participants with Pre-specified Adjudicated Cardiovascular Serious Adverse Events or Death from Any Cause | 12 weeks | |
| Number of Participants with Significant Increase in Blood Pressure | 12 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Percent Change from Baseline in High-density Lipoprotein-cholesterol (HDL-C) | Baseline and Week 12 | |
| Percent Change from Baseline in Apolipoprotein A-I (apoA-I) | Baseline and Week 12 |
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Inclusion Criteria:
with other lipid medications for at least 6 weeks
Exclusion Criteria:
(NYHA) Classes III or IV
lipids or lipoproteins
associated with malabsorption
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| Placebo | Drug | Placebo for anacetrapib orally, once daily for 12 weeks |
|
| ID | Term |
|---|---|
| D006938 | Hyperlipoproteinemia Type II |
| D000090542 | Homozygous Familial Hypercholesterolemia |
| ID | Term |
|---|---|
| D008052 | Lipid Metabolism, Inborn Errors |
| D008661 | Metabolism, Inborn Errors |
| D030342 | Genetic Diseases, Inborn |
| D009358 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities |
| D006951 | Hyperlipoproteinemias |
| D006949 | Hyperlipidemias |
| D050171 | Dyslipidemias |
| D052439 | Lipid Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| ID | Term |
|---|---|
| C530884 | anacetrapib |
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