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Lovaza Mechanisms of Action

Primary Purpose

Moderate Hypertriglyceridemia.

Status
Unknown status
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Omega 3 fatty acid (Lovaza)
Sponsored by
Brigham and Women's Hospital
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional basic science trial for Moderate Hypertriglyceridemia. focused on measuring Hypertriglyceridemia, Fish oil, Omega 3 fatty acids

Eligibility Criteria

21 Years - 65 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • Otherwise healthy 21 to 65 year old men and women
  • Triglycerides >150 < 500 mg/dL

Exclusion Criteria:

  • Other lipid lowering medication including fish oil
  • Major illnesses
  • Diabetes
  • Cardiovascular disease
  • Abnormalities uncovered on screening blood work including undiagnosed diabetes, abnormal liver function tests, triglycerides > 500 mg/dL
  • Indication for immediate statin therapy
  • Pregnancy
  • Contraindication for fish oil use or muscle biopsy

Sites / Locations

  • Brigham and Women's HospitalRecruiting

Outcomes

Primary Outcome Measures

Changes in lipoprotein metabolite content and their ability to activate PPAR-alpha in an established cell culture system.
Enrolled subjects will serve as their own controls and will be studied at baseline and after 3 months of Lovaza. The primary endpoint will test changes in lipoproteins as a function of their content and ability to activate PPAR-alpha in standard transfected cell culture systems.

Secondary Outcome Measures

Changes in plasma markers for atherosclerosis
Subjects will also be studied before and after Lovaza for changes in lipid profile and c- reactive protein
Change in plasma markers of diabetes
Plasma markers of diabetes will be measure before and after Lovaza treatment for 3 months, specifically glucose and A1C levels
Changes in plasma markers of liver function
Plasma levels of liver function tests, specifically ALT and AST before and after 3 months of Lovaza. This is not a safety issue since elevated triglycerides can cause increased liver function tests and fish oil (like Lovaza) can lower triglyceride levels and hence ALT and AST levels.

Full Information

First Posted
February 18, 2011
Last Updated
February 21, 2013
Sponsor
Brigham and Women's Hospital
Collaborators
GlaxoSmithKline
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1. Study Identification

Unique Protocol Identification Number
NCT01301794
Brief Title
Lovaza Mechanisms of Action
Official Title
Study of the Effects of Lovaza (Omega 3 Fatty Acids) On Lipoprotein Particles and Their Transcriptional Effects
Study Type
Interventional

2. Study Status

Record Verification Date
February 2013
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2013 (Anticipated)
Study Completion Date
August 2014 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Brigham and Women's Hospital
Collaborators
GlaxoSmithKline

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
High levels of triglycerides is a common abnormality found in patients with diabetes and also cardiovascular disease, and may contribute to the risk for both. Omega 3 fatty acids, as found enriched in fish and also in the commercial agent called Lovaza lower triglyceride levels. Prior work from the investigators group demonstrated that an enzyme responsible for the break down of triglycerides - lipoprotein lipase - generates molecules that can activate a specific nuclear receptor known as PPAR-alpha. This study investigates the hypothesis that taking Lovaza shifts the specific fatty acid content of triglyceride containing lipoproteins and increases the ability of those lipoproteins to activate PPAR-alpha.
Detailed Description
This study will investigate changes in lipid and other metabolic parameters as well as the ability of isolated lipoproteins to activate PPARs in the presence or absence of lipoprotein lipase in a cohort of normal healthy individuals with modest hypertriglyceridemia before and after a course of Lovaza.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Moderate Hypertriglyceridemia.
Keywords
Hypertriglyceridemia, Fish oil, Omega 3 fatty acids

7. Study Design

Primary Purpose
Basic Science
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
40 (Anticipated)

8. Arms, Groups, and Interventions

Intervention Type
Dietary Supplement
Intervention Name(s)
Omega 3 fatty acid (Lovaza)
Other Intervention Name(s)
Lovaza LVZ112737, formerly known as Omacor., Omega 3 fatty acids are also available over the counter but Lovaza is a proprietary form.
Intervention Description
Lovaza is an FDA approved omega 3 fatty acid taken as 4 grams a day (two one gram formulations twice a day).
Primary Outcome Measure Information:
Title
Changes in lipoprotein metabolite content and their ability to activate PPAR-alpha in an established cell culture system.
Description
Enrolled subjects will serve as their own controls and will be studied at baseline and after 3 months of Lovaza. The primary endpoint will test changes in lipoproteins as a function of their content and ability to activate PPAR-alpha in standard transfected cell culture systems.
Time Frame
3 months
Secondary Outcome Measure Information:
Title
Changes in plasma markers for atherosclerosis
Description
Subjects will also be studied before and after Lovaza for changes in lipid profile and c- reactive protein
Time Frame
3 months
Title
Change in plasma markers of diabetes
Description
Plasma markers of diabetes will be measure before and after Lovaza treatment for 3 months, specifically glucose and A1C levels
Time Frame
3 months
Title
Changes in plasma markers of liver function
Description
Plasma levels of liver function tests, specifically ALT and AST before and after 3 months of Lovaza. This is not a safety issue since elevated triglycerides can cause increased liver function tests and fish oil (like Lovaza) can lower triglyceride levels and hence ALT and AST levels.
Time Frame
3 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
21 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Otherwise healthy 21 to 65 year old men and women Triglycerides >150 < 500 mg/dL Exclusion Criteria: Other lipid lowering medication including fish oil Major illnesses Diabetes Cardiovascular disease Abnormalities uncovered on screening blood work including undiagnosed diabetes, abnormal liver function tests, triglycerides > 500 mg/dL Indication for immediate statin therapy Pregnancy Contraindication for fish oil use or muscle biopsy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Jorge Plutzky, MD
Phone
617-525-4360
Email
jplutzky@rics.bwh.harvard.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Jon Brown, MD
Phone
617-525-4360
Email
jbrown0@partners.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jorge Plutzky, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jonathan Brown, MD
Organizational Affiliation
Brigham and Women's Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Brigham and Women's Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Sutanuka Lahiri
Phone
617-525-6823
Email
Sutanuka Lahiri <SLAHIRI@PARTNERS.ORG>
First Name & Middle Initial & Last Name & Degree
Jorge Plutzky
Phone
326-055-200
Email
jplutzky@rics.bwh.harvard.edu

12. IPD Sharing Statement

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Lovaza Mechanisms of Action

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