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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 Oct 24, 2026, 10:05 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

Brief summary

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

The primary objective is to determine the efficacy of AMR101 (ethyl icosapentate) compared to placebo in lowering fasting triglyceride levels in patients with very high fasting triglyceride levels ≥ 500 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

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
Dec 2009 (Type not available)
Primary completion
Oct 2010 (Actual)
Completion
Jul 2011 (Actual)
Last update posted
Apr 25, 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 25, 2022 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01047683 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →