The purpose of this study is to determine if MSDC-0160 is effective in the treatment of Type 2 diabetes.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
86
Unnamed facility
Los Angeles, California, United States
Unnamed facility
Miami Gardens, Florida, United States
Unnamed facility
West Palm Beach, Florida, United States
Unnamed facility
Kalamazoo, Michigan, United States
Change From Baseline in Averaged Postprandial Glucose in Response to a MMT Test
Change from baseline of averaged postprandial glucose (mmol/L) in response to a Mixed-meal tolerance (MMT) test.
Time frame: 28 days
Change From Baseline in Averaged Insulin Levels in Response to a Mixed-meal Tolerance Test
Change from baseline in averaged post prandial insulin levels in response to a mixed-meal tolerance test.
Time frame: After four weeks of active therapy
Change From Baseline in FFAs
Change from baseline in Free Fatty Acids (FFAs)following 28 days of active therapy, as part of a lipid profile assessment
Time frame: After 28 days of active therapy
Change From Baseline in Triglycerides
Change compared to baseline in triglycerides following 28 days of active therapy, as part of a lipid profile assessment
Time frame: 28 days
Change From Baseline in HDL
Change from baseline in HDL following 28 days of active therapy, as part of a lipid profile assessment
Time frame: 28 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
Once daily, oral
Unnamed facility
Greenville, South Carolina, United States
Unnamed facility
Dallas, Texas, United States
Unnamed facility
San Antonio, Texas, United States
Unnamed facility
Renton, Washington, United States