drugset / Trial / NCT01556594

Safety and Efficacy of a Novel Glucagon Formulation in Type 1 Diabetic Patients Following Insulin-induced Hypoglycemia

NCT01556594

RandomizedCrossoverOpen-labelTreatment

Summary

In this study, participants with Type 1 diabetes received insulin through an infusion into a vein to reduce their blood glucose, and then received nasal glucagon (NG) or glucagon for injection under the skin, and their blood glucose was measured for 3 hours. The main objective of this study was to evaluate the safety and efficacy of intranasal and subcutaneous glucagon (SC) in reversing insulin-induced hypoglycemia in participants with type 1 diabetes.

Timeline

Start
2012-03
Primary completion
2012-07
Completion
2012-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Glucagon Peptide 1 mg Intranasal
Subject Glucagon Peptide 2 mg Intranasal
Subject Glucagon Peptide 3 mg Intranasal

Indications