drugset / Trial / NCT00545337

Glulisine + Lantus in Type I Patients

NCT00545337

Phase 3 Completed 60 enrolled Sanofi
Non-randomizedSingle-groupOpen-labelTreatment

Summary

To evaluate the efficacy (in terms of change HbA1c from baseline to endpoint) and safety (in terms of adverse events, clinical chemistry, lipids, hematology) of insulin glulisine (HMR 1964) in subjects with type I diabetes mellitus

Timeline

Start
2004-09
Primary completion
2005-06
Completion
2005-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin glulisine Protein / enzyme biologic Subcutaneous