To investigate the efficacy and safety of K-877 Extended Release (ER) 0.2 mg/day or 0.4 mg/day (once daily) for 12 weeks in dyslipidemia, using K-877 Immediate Release (IR) 0.2 mg/day (twice daily) as a control.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
356
K-877 ER 0.2 mg tablet
K-877 ER 0.4 mg tablet
K-877 IR 0.1 mg tablet
Institute Medical Corporation Hitomikai Motomachi Takatsuka Naika Clinic
Kanagawa, Japan
Medical Corporation Heishinkai OCROM Clinic
Osaka, Japan
Dojinkinenkai Meiwa Hospital
Tokyo, Japan
Efficacy : % change from baseline in fasting serum TG (mg/dL)
Time frame: 4, 8, and 12 week after administration
Efficacy : % change from baseline in fasting serum Total Cholesterol (mg/dL)
Time frame: 4, 8, and 12 week after administration
Efficacy : % change from baseline in fasting serum LDL-C (mg/dL)
Time frame: 4, 8, and 12 week after administration
Efficacy : % change from baseline in fasting serum HDL-C (mg/dL)
Time frame: 4, 8, and 12 week after administration
Efficacy : % change from baseline in fasting serum non-HDL-C (mg/dL)
Time frame: 4, 8, and 12 week after administration
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Fukuwa Clinic
Tokyo, Japan
Ikebukuro Metropolitan Clinic
Tokyo, Japan
Medical Corp. Seikoukai New Medical Research System Clinic
Tokyo, Japan
Medical Corporation Asbo Tokyo Asbo Clinic
Tokyo, Japan
Medical Corporation Chiseikai Tokyo Center Clinic
Tokyo, Japan
Medical Corporation Heishinkai ToCROM Clinic
Tokyo, Japan
Medical Corporation Yuhokai Miho Clinic
Tokyo, Japan
...and 1 more locations