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Efficacy Study of Diazoxide Choline to Treat Hypertriglyceridemia

Phase 2
Completed
Conditions
Hypertriglyceridemia
Dyslipidemia
Interventions
Registration Number
NCT01211847
Lead Sponsor
Essentialis, Inc.
Brief Summary

Once a day oral administration with DCCR helps lower triglycerides

Detailed Description

The population will consist of Statin-naive and Statin-treated subjects, all without diabetes mellitus, with fasting triglyceride levels in the range of ≥ 500 mg/dL and \< 1500 mg/dL.

Subjects will be randomly assigned to 1 of 2 treatment groups: DCCR and Placebo

Approximately 44 subjects will be enrolled in the study and stratified by Statin use at a 1:1 ratio in each treatment group,

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
44
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
PlaceboPlaceboPlacebo matching DCCR
DCCRDiazoxide Choline Controlled-Release TabletDCCR Treatment with 290 mg Diazoxide Choline
Primary Outcome Measures
NameTimeMethod
Triglyceride-lowering efficacy of DCCR84 days

Fasting triglycerides (percent change from Baseline to Day 84)

Secondary Outcome Measures
NameTimeMethod
Improvement in other lipid profiles with DCCR84 days

Apolipoprotein B (Apo B) (percent change from Baseline to Day 84) Fasting non-HDL cholesterol (percent change from Baseline to Day 84)

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