drugset / Trial / NCT00964262

A Study to Evaluate Safety and Pharmacokinetics/Pharmacodynamics of Sustained Release(SR) Exenatide

NCT00964262

Phase 1 Completed 34 enrolled Peptron, Inc.
RandomizedSingle-groupTriple-blindTreatment

Summary

The purpose of this study is to evaluate the safety, pharmacokinetics, and pharmacodynamics of SR exenatide (PT302) in healthy subjects.

Timeline

Start
2009-08
Primary completion
2010-10
Completion
2010-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Exenatide Peptide 0.5 mg Subcutaneous
Subject Exenatide Peptide 1 mg Subcutaneous
Subject Exenatide Peptide 2 mg Subcutaneous
Subject Exenatide Peptide 4 mg Subcutaneous