The purpose of this study is to obtain information on PK/PD, efficacy and safety of SHR3824 over 12 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
168
Chinese PLA General Hospital
Beijing, China
RECRUITINGAdjusted Mean Change in HbA1c Levels
Time frame: Baseline to Week 12
The number of volunteers with adverse events as a measure of safety and tolerability
Time frame: Baseline to Week 12
Adjusted Mean Change in Fasting Plasma Glucose
Time frame: Baseline to Week 12
Proportion of Participants Achieving Glycemic Response Defined as HbA1c <7%
Time frame: Baseline to Week 12
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