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
| Type | Name | Description |
|---|---|---|
| DRUG | Regular Human Insulin | Individual dose of RHI administered subcutaneously |
| DRUG | Lispro | Individual dose of lispro administered subcutaneously |
| DRUG | VIAject | Individual dose of VIAject administered subcutaneously |
| DRUG | VIAject 50% | Individual dose of VIAject 50% administered subcutaneously |
| DRUG | VIAject/Insulin Glargine | VIAject mixed wiht insulin glargine and administered subcutaneously |
| DRUG | Insulin Glargine/VIAject | Individual 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.