drugset / Trial / NCT02778113

A Study of Glucagon Administered in Different Forms and Routes to Healthy Adults

NCT02778113

RandomizedCrossoverSingle-blindBasic science

Summary

The main purpose of this study was to evaluate the safety and tolerability of nasal glucagon (NG). The study drug was delivered into the participant's nostril (intranasally) or was given as an injection just under the skin (subcutaneously) once in each of four study periods. The study lasted about 23 days for each participant.

Timeline

Start
2011-10
Primary completion
2011-10
Completion
2011-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Glucagon Peptide 0.5 mg Intranasal
Subject Glucagon Peptide 1 mg Intranasal
Subject Glucagon Peptide 2 mg Intranasal

Indications

No indication recorded.