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Completed Phase 3 Interventional Results available

Efficacy and Safety of AMR101 (Ethyl Icosapentate) in Patients With Fasting Triglyceride (Tg) Levels ≥ 500 and ≤ 2000 mg/dL

ClinicalTrials.gov ID: NCT01047683

Public ClinicalTrials.gov record NCT01047683. 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 Jul 22, 2026, 7:45 PM EDT

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

Official title

Evaluation of the Efficacy and Safety of AMR101 (Ethyl Icosapentate) in Patients With Fasting Triglyceride Levels ≥ 500 mg/dL and ≤ 2000 mg/dL

Study identification

NCT ID
NCT01047683
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Amarin Pharma Inc.
Industry
Enrollment
229 participants

Conditions and interventions

Interventions

  • AMR101 (ethyl icosapentate) - 4 g/day Drug
  • AMR101 (ethyl icosapentate) - 2 g/day Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years and older
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 30, 2009
Primary completion
Sep 30, 2010
Completion
Jun 30, 2011
Last update posted
Apr 24, 2022

2009 – 2011

United States locations

U.S. sites
18
U.S. states
11
U.S. cities
16
Facility City State ZIP Site status
Amarin Investigational Site Sacramento California 95823
Amarin Investigational Site Golden Colorado 80401
Amarin Investigational Site Miami Florida 33169
Amarin Investigational Site Miami Florida 33183
Amarin Investigational Site Ocala Florida 34471
Amarin Investigational Site Addison Illinois 27106
Amarin Investigational Site Chicago Illinois 60611
Amarin Investigational Site Louisville Kentucky 40213
Amarin Investigational Site Butte Montana 59701
Amarin Investigational Site Raleigh North Carolina 27527
Amarin Investigational Site Winston-Salem North Carolina 27103
Amarin Investigational Site Cincinnati Ohio 45212
Amarin Investigational Site Cincinnati Ohio 45219
Amarin Investigational Site Lyndhurst Ohio 44124
Amarin Investigational Site Tulsa Oklahoma 74136
Amarin Investigational Site Corpus Christi Texas 78404
Amarin Investigational Site Houston Texas 77030
Amarin Investigational Site Richmond Virginia 23294

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 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01047683, 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 Apr 24, 2022 · Synced Jul 22, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT01047683 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →