drugset / Trial / NCT01104701
A Study to Examine the Efficacy, Safety and Tolerability, and Pharmacokinetics of Exenatide Once Monthly Suspension
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | Exenatide | Peptide | 2 mg | Subcutaneous |
| Comparator | Exenatide | Peptide | 5 mg | Subcutaneous |
| Comparator | Exenatide | Peptide | 8 mg | Subcutaneous |
| Comparator | Exenatide | Peptide | 11 mg | Subcutaneous |