The objective of this study is to evaluate the efficacy and safety of teneligliptin 20 mg orally administered once daily for 24 weeks compared with placebo in patients with type 2 diabetes mellitus who have inadequate glycemic control with empaglyflozin and metformin
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
235
To be orally administered once daily
To be orally administered once daily
Seoul National University Hospital
Seoul, South Korea
Changes from baseline HbA1c at week 24
Time frame: Baseline (week 0) and week 24
Changes from baseline FPG at week 24
Time frame: Baseline (week 0) and week 24
Percentage of subjects achieving the HbA1c goals (HbA1c < 7.0% or < 6.5%) at week 24
Time frame: Baseline (week 0) and week 24
Changes from baseline in BMI at week 24
Time frame: Baseline (week 0) and week 24
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