The purpose of this study is to determine the efficacy and safety of DWP16001 compared to placebo in the treatment of type 2 diabetes mellitus.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
196
Daewoong pharmatceutical
Seoul, South Korea
RECRUITINGChange from baseline in HbA1c
Time frame: at 12 weeks
Change from baseline in FPG
Time frame: at week 4, 8, 12
The proportion of patients who achieve HbA1c < 7.0%, HbA1c < 6.5% and HbA1c reduction >0.5% from baseline
Time frame: at week 4, 8, 12
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