Primary: * To investigate the efficacy of insulin glargine (in terms of change in A1c from baseline to endpoint A1c \< 7%) Secondary: * To investigate the safety of insulin glargine (in terms of hypoglycaemia, including symptomatic, non-symptomatic and nocturnal hypoglycaemia) * To investigate whether beta cell function is preserved if this therapy is initiated before 2nd OAD (oral anti-diabetic drug) failure
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
387
Throughout study period
Combination throughout the study period. Titrate to FPG ≤ 100 mg/dl.
Combination throughout the study period. Titrate to FPG ≤ 100 mg/dl.
Sanofi-Aventis
Beijing, China
A1c values
Time frame: At baseline and 24 weeks
Adverse events including hypoglycemia
Time frame: From the beginning to the end of the study
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Combination throughout the study period. Titrate to FPG ≤ 100 mg/dl.
Combination throughout the study period. Titrate to FPG ≤ 100 mg/dl.
Combination throughout the study period. Titrate to FPG ≤ 100 mg/dl.