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

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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.

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.

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
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520
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Rapid City, SD
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Akron, OH
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1157
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Anaheim, CA
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Birmingham, AL
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Brockton, MA
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8650
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Camperdown,
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Chevy Chase, MD
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610
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Chicago, IL
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726
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Cincinnati, OH
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1134
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Columbia, MD
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DeLand, FL
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Duncansville, Pennsylvania 16635
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1139
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Encinitas, CA
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1189
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Endwell, NY
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635
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Fargo, ND
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569
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Houston, TX
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643
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Indianapolis, IN
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1053
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Jacksonville, FL
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971
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Las Vegas, NV
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372
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Little Rock, AR
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657
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Louisville, KY
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Mount Pleasant, South Carolina 29464
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Mount Pleasant, SC
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1288
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New Windsor, NY
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Norman, OK
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Olive Branch, Mississippi 38654
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Olive Branch, MS
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Ponte Vedra, FL
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Raleigh, NC
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Renton, WA
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Saint Paul, MN
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Savannah, GA
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Seattle, WA
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Spring Valley, California 91978
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Spring Valley, CA
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Westlake Village, California 91361
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Westlake Village, CA
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