drugset / Trial / NCT00313183

A Study to Evaluate Symlin in Adolescent Subjects With Type 1 Diabetes Mellitus

NCT00313183

Phase 2 Completed 12 enrolled AstraZeneca
RandomizedCrossoverSingle-blindTreatment

Summary

This study will be the first evaluation of Symlin in adolescent subjects with type 1 diabetes mellitus and is designed to evaluate the blood levels (pharmacokinetics), biochemical and physiological effects (pharmacodynamics), and safety and tolerability of Symlin in these subjects.

Timeline

Start
2006-04
Primary completion
2007-08
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Pramlintide Peptide 15 ug Subcutaneous
Subject Pramlintide Peptide 30 ug Subcutaneous