The purpose of this study is to obtain information on efficacy and safety of SHR3824 over 24 weeks and 52 weeks in Chinese patients with Type 2 Diabetes. This will be done by comparing the effect of SHR3824 to placebo when given in oral doses.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
450
Chinese PLA General Hospital
Beijing, China
Adjusted Mean Change in HbA1c Levels
Time frame: Baseline to Week 24
The number of volunteers with adverse events as a measure of safety
Time frame: Baseline to Week 52
Adjusted Mean Change in Fasting Plasma Glucose
Time frame: Baseline to Week 24
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