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Completed Phase 3 Interventional Results available

Goal Achievement After Utilizing an Anti-PCSK9 Antibody in Statin Intolerant Subjects -2

ClinicalTrials.gov ID: NCT01763905

Public ClinicalTrials.gov record NCT01763905. 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 26, 2026, 10:58 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 Double-blind, Randomized, Multicenter Study to Evaluate Safety and Efficacy of AMG 145, Compared With Ezetimibe, in Hypercholesterolemic Subjects Unable to Tolerate an Effective Dose of a HMG-CoA Reductase Inhibitor

Brief summary

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

The primary objective was to evaluate the effect of 12 weeks of subcutaneous (SC) evolocumab every 2 weeks (Q2W) and monthly (QM), compared with ezetimibe, on percent change from baseline in low-density lipoprotein cholesterol (LDL-C) in hypercholesterolemic adults unable to tolerate an effective dose of a statin (HMG-CoA (5-hydroxy-3-methylglutaryl-coenzyme A) reductase inhibitors).

Study identification

NCT ID
NCT01763905
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amgen
Industry
Enrollment
307 participants

Conditions and interventions

Conditions

Interventions

Biological · Drug

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
Jan 24, 2013 (Actual)
Primary completion
Nov 19, 2013 (Actual)
Completion
Nov 19, 2013 (Actual)
Last update posted
Jul 20, 2020

2013

United States locations

U.S. sites
20
U.S. states
11
U.S. cities
18
Facility City State ZIP Site status
Research Site Carmichael California 95608 —
Research Site Los Angeles California 90048 —
Research Site Mission Viejo California 92691 —
Research Site Thousand Oaks California 91360 —
Research Site Atlanta Georgia 30338 —
Research Site Atlanta Georgia 30342 —
Research Site Savannah Georgia 31406 —
Research Site Auburn Maine 04210 —
Research Site Traverse City Michigan 49684 —
Research Site St Louis Missouri 63110 —
Research Site Henderson Nevada 89052 —
Research Site Las Vegas Nevada 89117 —
Research Site Las Vegas Nevada 89148 —
Research Site New York New York 10029 —
Research Site Raleigh North Carolina 27609 —
Research Site Akron Ohio 44311 —
Research Site Cincinnati Ohio 45212 —
Research Site Cleveland Ohio 44195 —
Research Site Norman Oklahoma 73069 —
Research Site Houston Texas 77030 —

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 38 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01763905, 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 Jul 20, 2020 · Synced Oct 26, 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 NCT01763905 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →