The purpose of this study is to determine the effect of JTT-302 on the increase of High Density Lipoprotein-Cholesterol (HDL-C) levels when administered daily for four weeks in subjects with low HDL-C levels.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
TRIPLE
Enrollment
150
Unnamed facility
Santa Ana, California, United States
Percent change from baseline in HDL-C at Week 4
Time frame: 4 weeks
Percent change and change from baseline at week 4 in lipid parameters
Time frame: 4 weeks
Evaluate the safety profile of JTT-302 when administered for 4 weeks
Time frame: 4 weeks
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