drugset / Trial / NCT00862849

Pharmacokinetic and Glucodynamic Crossover Study of Subcutaneously (SC) Administered Insulin Lispro + Recombinant Human Hyaluronidase (rHuPH20) and Regular Human Insulin + rHuPH20 Compared to Insulin Lispro Alone

NCT00862849

Phase 1 Completed 22 enrolled Halozyme Therapeutics
CrossoverDouble-blind

Summary

Insulin lispro and regular human insulin are Food and Drug Administration (FDA)-approved medications for the treatment of diabetes mellitus. Recombinant human hyaluronidase (rHuPH20) is approved by the FDA as an aid to the absorption and dispersion of other injectable drugs. In this study, rHuPH20 will be co-administered with both insulin lispro and regular human insulin in order to determine if it improves the absorption of these insulins to more closely mimic the body's natural increase in insulin in response to a meal.

Timeline

Start
2009-03
Primary completion
2009-06
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Insulin Protein / enzyme biologic 0.15 iu/kg Subcutaneous
Subject Insulin Lispro Protein / enzyme biologic 0.15 iu/kg Subcutaneous
Subject rHuPH20 Protein / enzyme biologic 3.75 ng Subcutaneous

Indications