To investigate the glycosylated hemoglobin (HbA1c) control of Glimepiride (AMARYL) as OAD
initiation mono-therapy in type 2 diabetic patients in China.
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Full eligibility criteria for NCT00908921
Ages eligible for Study
18 Years and older
Genders eligible for Study
Accepts Healthy Volunteers
Newly diagnosed T2DM and inadequately controlled with diet and exercise or T2DM diagnosed <6 months and who had not taken oral antidiabetic medication or insulin for
HbA1C more than 7.5 and less than 11.
Fasting plasma glucose of >13.5mmol/L
Type 1 Diabetes Mellitus (T1DM)
Patient with acute illness hospitalized in last 2 months
Patient with active liver disease, impaired renal or hepatic functions
Known hypersensitivity to glimepiride, other sulfonylureas, other sulfonamides or any other excipients of AMARYL
Pregnant and lactating women The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.
All locations for NCT00908921
Sanofi-Aventis Administrative Office
View full eligibility
Tris trial is registered with FDA with number: NCT00908921. The sponsor of the trial is Sanofi and it is looking for 391 volunteers for the current phase.
Official trial title: Efficacy and Safety of Glimepiride as Oral Anti-Diabetic (OAD) Initiation Mono- Therapy in Chinese Type 2 Diabetes Mellitus (T2DM)
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