The purpose of this study is to determine the effect of gemcabene on insulin sensitivity as defined by average glucose disposal rate.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
QUADRUPLE
Enrollment
53
Gemcabene 900 mg once daily (QD)
Placebo
Insulin sensitivity
Time frame: 4 weeks
Adverse Events
Time frame: 4 weeks
ECG
Clinically Significant Changes
Time frame: 4 weeks
Clinical Laboratory - hematology, chemistry
Clinical Laboratory Abnormalities
Time frame: 4 weeks
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