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Completed Phase 3 Interventional Results available

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

ClinicalTrials.gov ID: NCT02304484

Public ClinicalTrials.gov record NCT02304484. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 27, 2026, 12:27 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

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.

Study identification

NCT ID
NCT02304484
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
770 participants

Conditions and interventions

Interventions

Biological

Eligibility (public fields only)

Age range
18 Years to 99 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 24, 2014 (Actual)
Primary completion
Mar 9, 2018 (Actual)
Completion
Mar 9, 2018 (Actual)
Last update posted
Mar 19, 2019

2014 – 2018

United States locations

U.S. sites
24
U.S. states
15
U.S. cities
24
Facility City State ZIP Site status
Research Site Huntsville Alabama 35801 —
Research Site Mobile Alabama 36608 —
Research Site Long Beach California 90822 —
Research Site San Diego California 92161 —
Research Site Torrance California 90502 —
Research Site Jacksonville Florida 32216 —
Research Site Munster Indiana 46321 —
Research Site Lexington Kentucky 40536 —
Research Site Covington Louisiana 70433 —
Research Site Bethesda Maryland 20814 —
Research Site Columbia Maryland 21044 —
Research Site Bay City Michigan 48708 —
Research Site Midland Michigan 48670 —
Research Site Duluth Minnesota 55805 —
Research Site Saint Cloud Minnesota 56303 —
Research Site Columbia Missouri 65212 —
Research Site Ridgewood New Jersey 07450 —
Research Site Fargo North Dakota 58122 —
Research Site Canton Ohio 44710 —
Research Site Toledo Ohio 43614 —
Research Site Oak Ridge Tennessee 37830 —
Research Site Amarillo Texas 79106 —
Research Site Dallas Texas 75216 —
Research Site Wichita Falls Texas 76301 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 102 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02304484, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 19, 2019 · Synced Oct 27, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT02304484 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →