The purpose of this study is to evaluate the efficacy and safety of 3 different doses of SHR3824 compared with placebo in patients with type 2 diabetes mellitus who are receiving treatment with metformin monotherapy (ie, treatment with a single drug) and have inadequate glycemic (blood sugar) control.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
168
Adjusted 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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