Study identifier:2993LAR-104
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Multicenter Study to Examine Safety and Pharmacokinetics of Exenatide Long-Acting Release Administered Weekly in Subjects with Type 2 Diabetes Mellitus
Type 2 Diabetes Mellitus
Phase 2
No
placebo, Exenatide LAR
All
45
Interventional
18 Years - 75 Years
Allocation: Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Jan 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
Eli Lilly and Company
No locations available
Arms | Assigned Interventions |
---|---|
Placebo Comparator: Group A1 Placebo lead-in followed by placebo equivalent volume to 0.8 mg exenatide LAR | Drug: placebo Subcutaneously injected placebo 0.02 mL twice daily as lead-in followed by once weekly injected amount equivalent to exenatide LAR 0.8 mcg |
Placebo Comparator: Group A2 Placebo lead-in followed by placebo equivalent volume to 2.0 mg exenatide LAR | Drug: placebo Subcutaneously injected placebo 0.02 mL twice daily as lead-in followed by once weekly injected amount equivalent to exenatide LAR 2.0 mcg |
Experimental: Group B Exenatide lead-in followed by exenatide LAR 0.8 mg weekly | Drug: Exenatide LAR Subcutaneously injected exenatide 5 mcg (0.02 mL) twice daily as lead-in followed by once weekly injected exenatide LAR 0.8 mcg. Other Name: Bydureon |
Experimental: Group C Exenatide lead-in followed by exenatide LAR 2.0 mg weekly | Drug: Exenatide LAR Subcutaneously injected exenatide 5 mcg (0.02 mL) twice daily as lead-in followed by once weekly injected exenatide LAR 2.0 mcg. Other Name: Bydureon |