Open-label Extension (OLE) Study to Assess Safety and Efficacy of Evolocumab



Status:Completed
Conditions:High Cholesterol
Therapuetic Areas:Cardiology / Vascular Diseases
Healthy:No
Age Range:18 - 99
Updated:3/21/2019
Start Date:November 24, 2014
End Date:March 9, 2018

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A Multicenter, Open-label Extension (OLE) Study to Assess the Long-term Safety and Efficacy of Evolocumab

The purpose of this study was to characterize the safety and tolerability of long-term
administration of evolocumab in adults with known coronary artery disease and
hypercholesterolemia.


Inclusion Criteria:

- Completed week 80 of study 20120153 (NCT01813422).

Exclusion Criteria:

- Did not complete investigational product in the 20120153 parent study

- Have an unstable medical condition, in the judgment of the investigator

- Known sensitivity to any of the products to be administered during dosing

- Currently enrolled in another investigational device or drug study (excluding
evolocumab (AMG 145) parent study), or less than 30 days since ending another
investigational device or drug study(s),or receiving other investigational agent(s)
We found this trial at
25
sites
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Fargo, ND
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Amarillo, TX
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Bay City, MI
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Bethesda, MD
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Canton, OH
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Columbia, MD
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Columbia, MO
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Covington, LA
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from
Dallas, TX
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from
Duluth, MN
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from
Huntsville, AL
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Jacksonville, FL
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La Plata,
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Lexington, KY
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Long Beach, CA
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Midland, MI
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from
Mobile, AL
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from
Munster, IN
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from
Oak Ridge, TN
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from
Ridgewood, NJ
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from
Saint Cloud, MN
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San Diego, CA
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from
Toledo, OH
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from
Torrance, CA
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from
Wichita Falls, TX
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