Placebo Controlled Study Using Lovaza as Treatment for Non-Alcoholic Fatty Liver Disease

PHASE4UnknownINTERVENTIONAL
Enrollment

40

Participants

Timeline

Start Date

September 30, 2009

Primary Completion Date

September 30, 2012

Study Completion Date

September 30, 2012

Conditions
Non-Alcoholic Fatty Liver Disease
Interventions
DRUG

Lovaza

Approximately 50% of study subjects will be randomized to the active treatment arm -Lovaza. Subjects will be dosed with 4g of Lovaza gel capsules daily for a minimum of 48 weeks duration.

DRUG

placebo control

Approximately 50% of study subjects will be randomized to the placebo arm of this study. Placebo arm subjects will receive 4g of placebo gel caps daily for a minimum of 48 weeks duration.

Trial Locations (1)

91105

RECRUITING

HMRI - Liver Center, Pasadena

Sponsors
All Listed Sponsors
collaborator

GlaxoSmithKline

INDUSTRY

lead

Huntington Medical Research Institutes

OTHER