ELEONOR STUDY: Insulin Glulisine in Type 2 Diabetes Mellitus.

PHASE3CompletedINTERVENTIONAL
Enrollment

352

Participants

Timeline

Start Date

October 31, 2005

Primary Completion Date

May 31, 2008

Study Completion Date

May 31, 2008

Conditions
Diabetes Mellitus, Type 2
Interventions
DRUG

Insulin glulisine

individualized, once daily, dose aiming at 2h post-prandial plasma glucose goal \< 140 mg/dl (7.8 mmol/l) in the optimized treatment phase, since visit 3, subcutaneous

DRUG

Insulin glargine

individualized, once daily, dose to reach mean fasting plasma glucose (FPG) \<= 126 mg/dl (7.0 mmol/l), since randomization, subcutaneous

DRUG

Metformin

1000 mg b.i.d, since the qualification phase, oral

Trial Locations (1)

Unknown

Sanofi-Aventis Administrative Office, Milan

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Sanofi

INDUSTRY

NCT00272064 - ELEONOR STUDY: Insulin Glulisine in Type 2 Diabetes Mellitus. | Biotech Hunter | Biotech Hunter