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Completed Phase 3 Interventional Results available

Study to Assess In-home Use of Evolocumab (AMG 145) Using a Prefilled Syringe or a Prefilled Autoinjector/Pen

ClinicalTrials.gov ID: NCT01849497

Public ClinicalTrials.gov record NCT01849497. 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 21, 2026, 9:38 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 Multi-center, Randomized Study in Subjects With Primary Hypercholesterolemia or Mixed Dyslipidemia to Assess Subjects' Ability to Administer a Full Dose of Evolocumab (AMG 145) in Home-use, Using Either a Prefilled Syringe or a Prefilled Autoinjector/Pen

Brief summary

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

The primary objective of this study was to assess users' ability to administer a full dose of evolocumab in home-use using either a pre-filled syringe or autoinjector/pen.

Study identification

NCT ID
NCT01849497
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
149 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 80 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
Apr 18, 2013 (Actual)
Primary completion
Sep 2, 2013 (Actual)
Completion
Not listed
Last update posted
Nov 29, 2018

Started 2013

United States locations

U.S. sites
21
U.S. states
12
U.S. cities
20
Facility City State ZIP Site status
Research Site Encino California 91436 —
Research Site Thousand Oaks California 91360 —
Research Site Ventura California 93003 —
Research Site Westlake Village California 91361 —
Research Site Miami Florida 33173 —
Research Site Port Charlotte Florida 33952 —
Research Site Atlanta Georgia 30328 —
Research Site Atlanta Georgia 30342 —
Research Site Hammond Indiana 46320 —
Research Site Auburn Maine 04210 —
Research Site Manlius New York 13104 —
Research Site Syracuse New York 13210 —
Research Site Cadiz Ohio 43907 —
Research Site Marion Ohio 43302 —
Research Site Hillsboro Oregon 97123 —
Research Site Duncansville Pennsylvania 16635 —
Research Site Lansdale Pennsylvania 19446 —
Research Site Rapid City South Dakota 57701 —
Research Site Jackson Tennessee 38305 —
Research Site Dallas Texas 75231 —
Research Site Houston Texas 77074 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01849497, 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 Nov 29, 2018 · Synced Oct 21, 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 NCT01849497 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →