ClinicalTrials.gov record
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 May 20, 2026, 11:43 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

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

  • Evolocumab Biological
  • Ezetimibe Drug
  • Placebo to Evolocumab Drug
  • Placebo to Ezetimibe Drug

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 23, 2013
Primary completion
Nov 18, 2013
Completion
Nov 18, 2013
Last update posted
Jul 19, 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 19, 2020 · Synced May 20, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01763905 live on ClinicalTrials.gov.

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