drugset / Trial / NCT00460304

The Effect of Pramlintide on Meal Time Insulin Bolus

NCT00460304

Non-randomizedSingle-groupOpen-labelTreatment

Summary

The primary objective is to establish the mean percentage of change in the insulin-to-carbohydrate ratio due to pramlintide treatment once a maximum tolerated dose or 6 mcg before each meal is reached. The secondary objective is to establish which insulin bolus wave form is associated with the lowest post-bolus without hypoglycemia in subjects treated with maximum pramlintide dosage.

Timeline

Start
2007-09
Primary completion
2008-11
Completion
2008-11

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramlintide Peptide 6 ug