A study to compare the efficacy, safety, and pharmacokinetics of K-877 controlled release tablets with a current normal K-877 tablet in dyslipidemia.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Enrollment
60
K-877 IR 0.1 mg tablet
K-877 CR 0.4 mg tablet
Two K-877 CR 0.4 mg tablet
Medical Corporation Heishinkai OPHAC Hospital
Osaka, Japan
Efficacy: % change from baseline in fasting serum TG(mg/dL)
Time frame: 4 week after administration in each period
% change from baseline in fasting HDL-C levels(mg/dL)
Time frame: 4 week after administration in each period
% change from baseline in fasting LDL-C levels(mg/dL)
Time frame: 4 week after administration in each period
% change from baseline in fasting non-HDL-C levels(mg/dL)
Time frame: 4 week after administration in each period
% change from baseline in fasting Total Cholesterol levels(mg/dL)
Time frame: 4 week after administration in each period
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