drugset / Trial / NCT01156779

Study to Evaluate Safety and PK/PD of DA-3091 in Healthy Male Subjects

NCT01156779 ↗

Phase 1 Completed 31 enrolled Dong-A Pharmaceutical Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

This Phase I clinical study is to evaluate the safety and tolerance of DA-3091 and to characterize the pharmacokinetic/pharmacodynamic of DA-3091 in healthy male subjects

Timeline

Start
2010-07
Primary completion
2012-04
Completion
—

Drugs

EvaluationDrugModalityDoseRoute
Subject SR-exenatide Unknown 0.5 mg Subcutaneous
Subject SR-exenatide Unknown 1 mg Subcutaneous
Subject SR-exenatide Unknown 2 mg Subcutaneous
Subject SR-exenatide Unknown 4 mg Subcutaneous

Indications