The purpose of this study is to assess the safety and effectiveness of three doses of CKD-501 compared to placebo in lowering fasting plasma glucose levels in people with type 2 diabetes for 8 weeks.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
214
0.5 mg/tablet, orally, 1 tablet once daily for 8 weeks
1 mg/tablet, orally, 1 tablet once daily for 8 weeks
2 mg/tablet, orally, 1 tablet once daily for 8 weeks
The Inje University Medical Center
Busan, South Korea
The Yeungnam University Hospital
Daegu, South Korea
The Chtholic University of Korea Uijeongbu St. Mary's Hospital
Gyeonggi-do, South Korea
The Seoul National Univertisy Bundang Hospital
Gyeonggi-do, South Korea
Change from baseline in fasting plasma glucose at 8 weeks
Time frame: 8 weeks
Change from baseline in Glycemic parameters after 8 weeks
Time frame: 8 weeks
Change from baseline in Lipid parameters after 8 weeks
Time frame: 8 weeks
Adverse event profile after 8 weeks of treatment
Time frame: 8 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
orally, 1 tablet once daily for 8 weeks
The Wonju Christian Hospital
Kangwon-Do, South Korea
The Inje University Sanggye-Paik Hospital
Seoul, South Korea
The Korea University Anam Hospital
Seoul, South Korea
The Samsung Medical Center
Seoul, South Korea