drugset / Trial / NCT01297062

A Safety Study to Assess the Effects of Therapeutic and Supratherapeutic Exenatide Concentrations on QT Interval in Healthy Subjects

NCT01297062

Phase 1 Completed 94 enrolled AstraZeneca Eli Lilly and Company · collab
RandomizedCrossoverTriple-blind

Summary

Compare the effect of exenatide (therapeutic and supratherapeutic concentrations), moxifloxacin and placebo on the QT interval.

Timeline

Start
2011-02
Primary completion
2011-04
Completion
2011-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Exenatide Peptide Intravenous
Comparator Moxifloxacin Small molecule 400 mg Oral

Indications

No indication recorded.