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A Double-blind Randomized Placebo-controlled Study Comparing Epanova and Fenofibrate on Liver Fat in Overweight Subjects.

AstraZeneca logo

AstraZeneca

Status and phase

Completed
Phase 2

Conditions

Non-alcoholic Fatty Liver Disease (NAFLD
Hypertriglyceridemia

Treatments

Drug: Omega-3 carboxylic acid
Drug: Fenofibrate 200mg
Drug: Placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT02354976
D5881C00007

Details and patient eligibility

About

This study is a double-blind randomized, placebo-controlled, parallel-group, 12 week study performed in 2 centres in Sweden to assess the effect of Omega-3 carboxylic acids and fenofibrate on liver fat measured with magnetic resonance imaging (MRI) in patients with over-weight and hypertriglyceridemia.

Enrollment

78 patients

Sex

All

Ages

40 to 75 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria: - Provision of informed consent

  • Men or women ≥40 years and ≤75 years with suitable veins for cannulation or repeated venepuncture

  • Have serum triglycerides ≥1.7 mM

  • Have liver fat content as assessed by MRI >5.5%

  • Have a body mass index (BMI) >25 and ≤40 kg/m2

    , Exclusion Criteria: - History of or presence of any clinically significant disease or disorder which, in the opinion of the investigator, may either put the subject at risk because of participation in the study, or influence the results or the subject's ability to participate in the study.

  • Creatinine clearance <60 mL/min at screening (Cockcroft-Gault formula).

  • Severe hepatic insufficiency and/or significant abnormal liver function defined as aspartate aminotransferase (AST) >3x upper limit of normal (ULN) and/or alanine aminotransferase (ALT) >3x ULN

  • Total bilirubin >2.0 mg/dL (34.2 µmol/L)

  • Type 2 diabetes, as defined by WHO criteria e.g. fasting plasma Glucose >7.0 mM or use of antidiabetic therapy

  • Any clinically significant abnormalities in clinical chemistry, haematology or urinalysis results as judged by the investigator. This includes signs of liver disease other than NAFLD that motivates further investigations of treatment based on clinical judgement

  • Recent history (past 12 months) of drug abuse or alcohol abuse. Alcohol abuse was to be defined as >14 drinks per week (1 drink = 35 cl beer, 14 cl wine, or 4 cl hard liquor) or as judged by the investigator

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

78 participants in 3 patient groups, including a placebo group

Placebo
Placebo Comparator group
Treatment:
Drug: Placebo
Drug: Placebo
Omega-3 carboxylic acids 4g / day
Experimental group
Treatment:
Drug: Omega-3 carboxylic acid
Fenofibrate 200mg
Active Comparator group
Treatment:
Drug: Fenofibrate 200mg

Trial contacts and locations

4

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Data sourced from clinicaltrials.gov

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