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

Outcome

Met primary endpoint

registry Least Squares Mean Difference -1.36 (90% CI -2.21 to -0.50) NCT01297062 ↗

registry Least Squares Mean Difference -2.02 (90% CI -2.88 to -1.16) NCT01297062 ↗

registry Least Squares Mean Difference -1.13 (90% CI -2.11 to -0.15) NCT01297062 ↗

Drugs

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

Indications

No indication recorded.