drugset / Trial / NCT01104701

A Study to Examine the Efficacy, Safety and Tolerability, and Pharmacokinetics of Exenatide Once Monthly Suspension

NCT01104701

Phase 2 Completed 121 enrolled AstraZeneca Eli Lilly and Company · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of Study BCB111 is to collect efficacy, pharmacokinetic, pharmacodynamic, safety, and tolerability data in patients with type 2 diabetes to assess the feasibility of once monthly dosing of the exenatide suspension formulation.

Timeline

Start
2010-05
Primary completion
2010-12
Completion
2010-12

Drugs

EvaluationDrugModalityDoseRoute
Comparator Exenatide Peptide 2 mg Subcutaneous
Comparator Exenatide Peptide 5 mg Subcutaneous
Comparator Exenatide Peptide 8 mg Subcutaneous
Comparator Exenatide Peptide 11 mg Subcutaneous