Expanded PK and PD of Insulin Glulisine Versus Insulin Aspart in Healthy Volunteers

PHASE1CompletedINTERVENTIONAL
Enrollment

12

Participants

Timeline

Start Date

November 30, 2007

Primary Completion Date

December 31, 2007

Study Completion Date

June 30, 2008

Conditions
Diabetes
Interventions
DRUG

insulin glulisine, insulin aspart

single subcutaneous dose of 0.2 units per kg body weight of insulin glulisine during first euglycemic glucose clamp, single subcutaneous dose of 0.2 units per kg body weight of insulin aspart during second euglycemic glucose clamp

DRUG

insulin aspart, insulin glulisine

single subcutaneous dose of 0.2 units per kg body weight of insulin aspart during first euglycemic glucose clamp, single subcutaneous dose of 0.2 units per kg body weight of insulin glulisine during second euglycemic glucose clamp

Trial Locations (1)

D-41460

Profil Institut für Stoffwechselforschung GmbH, Neuss

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Sanofi

INDUSTRY

lead

Profil Institut für Stoffwechselforschung GmbH

INDUSTRY

NCT00969592 - Expanded PK and PD of Insulin Glulisine Versus Insulin Aspart in Healthy Volunteers | Biotech Hunter | Biotech Hunter