Clinical Trials Directory

Trials / Completed

CompletedNCT01000922

A Study Comparing the Pharmacodynamic Properties of Insulin VIAJECT™, Regular Human Insulin, and Insulin Lispro

A Single Center, Randomized, Open-Label, Crossover Study, Comparing the Pharmacodynamic Properties of Insulin VIAJECT™, Regular Human Insulin, and Insulin Lispro Either in Combination With a Basal Insulin Infusion or With Insulin Glargine Relative to a Standardized Meal in Patients With Type 1 Diabetes

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
24 (actual)
Sponsor
Biodel · Industry
Sex
All
Age
19 Years – 70 Years
Healthy volunteers
Not accepted

Summary

Evaluation of post-prandial blood glucose excursions after a standardized meal and pre meal injections of individual doses of the study insulins.

Conditions

Interventions

TypeNameDescription
DRUGRegular Human InsulinIndividual dose of RHI administered subcutaneously
DRUGLisproIndividual dose of lispro administered subcutaneously
DRUGVIAjectIndividual dose of VIAject administered subcutaneously
DRUGVIAject 50%Individual dose of VIAject 50% administered subcutaneously
DRUGVIAject/Insulin GlargineVIAject mixed wiht insulin glargine and administered subcutaneously
DRUGInsulin Glargine/VIAjectIndividual dose of VIAject and Insulin Glargine administered seperately and subcutaneously

Timeline

Start date
2006-06-01
Primary completion
2008-01-01
Completion
2008-01-01
First posted
2009-10-23
Last updated
2015-07-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01000922. Inclusion in this directory is not an endorsement.