Durable Effect of PCSK9 Antibody CompARed wiTh placEbo Study
Status: | Completed |
---|---|
Conditions: | High Cholesterol |
Therapuetic Areas: | Cardiology / Vascular Diseases |
Healthy: | No |
Age Range: | 18 - 80 |
Updated: | 11/30/2018 |
Start Date: | January 5, 2012 |
End Date: | October 14, 2013 |
A Double-Blind, Randomized, Placebo-controlled, Multicenter Study to Evaluate Long-Term Tolerability and Durable Efficacy of AMG 145 (Evolocumab) on LDL-C in Hyperlipidemic Subjects
To evaluate the efficacy, safety, and tolerability of 52 weeks of subcutaneous (SC)
evolocumab (AMG 145) compared with placebo when added to assigned background lipid-lowering
therapy.
evolocumab (AMG 145) compared with placebo when added to assigned background lipid-lowering
therapy.
Eligible participants with screening central laboratory low-density lipoprotein cholesterol
(LDL-C) values ≥ 75 mg/dL (1.9 mmol/L) were instructed to follow National Cholesterol
Education Program (NCEP) Adult Treatment Panel III (ATP) Therapeutic Lifestyle Changes (TLC)
diet and were assigned to 1 of the following 4 background lipid-lowering therapies for a
4-week stabilization period based upon their screening LDL-C and its distance from the
individual's required goal as stipulated by their NCEP ATP III risk category:
1. no drug therapy required - diet alone
2. low dose drug therapy required - diet plus atorvastatin 10 mg orally (PO) once daily
(QD)
3. high dose drug therapy required - diet plus atorvastatin 80 mg PO QD
4. maximal drug therapy required - diet plus atorvastatin 80 mg PO QD plus ezetimibe 10 mg
PO QD.
If the participant met entry criteria at the end of the lipid stabilization period they were
randomized 2:1 to receive evolocumab 420 mg or placebo subcutaneously once a month for 52
weeks in addition to their background therapy.
(LDL-C) values ≥ 75 mg/dL (1.9 mmol/L) were instructed to follow National Cholesterol
Education Program (NCEP) Adult Treatment Panel III (ATP) Therapeutic Lifestyle Changes (TLC)
diet and were assigned to 1 of the following 4 background lipid-lowering therapies for a
4-week stabilization period based upon their screening LDL-C and its distance from the
individual's required goal as stipulated by their NCEP ATP III risk category:
1. no drug therapy required - diet alone
2. low dose drug therapy required - diet plus atorvastatin 10 mg orally (PO) once daily
(QD)
3. high dose drug therapy required - diet plus atorvastatin 80 mg PO QD
4. maximal drug therapy required - diet plus atorvastatin 80 mg PO QD plus ezetimibe 10 mg
PO QD.
If the participant met entry criteria at the end of the lipid stabilization period they were
randomized 2:1 to receive evolocumab 420 mg or placebo subcutaneously once a month for 52
weeks in addition to their background therapy.
Inclusion Criteria:
- Subject has provided informed consent.
- Fasting LDL-C ≥ 75 mg/dL and meeting the following LDL-C values on background
lipid-lowering therapy:
- < 100 mg/dL for subjects with diagnosed coronary heart disease (CHD) or CHD risk
equivalent
- < 130 mg/dL for subjects without diagnosed CHD or CHD risk equivalent
- OR on maximal background lipid-lowering therapy defined as atorvastatin 80 mg PO
QD and ezetimibe 10 mg PO QD
- Fasting triglycerides ≤ 400 mg/dL
Exclusion Criteria:
- New York Heart Association (NYHA) II-IV heart failure, or last known left ventricular
ejection fraction < 30%
- Uncontrolled cardiac arrhythmia
- Myocardial infarction, unstable angina, percutaneous coronary intervention (PCI),
coronary artery bypass graft (CABG) or stroke within 3 months prior to randomization,
type 1 diabetes, newly diagnosed or poorly controlled type 2 diabetes
- Uncontrolled hypertension
We found this trial at
37
sites
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