Study identifier:137-156
ClinicalTrials.gov identifier:N/A
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Double-Blind, Placebo-Controlled, Multicenter Study Evaluating the Efficacy and Safety of Adding Symlin® to Lantus® (Insulin Glargine) in Subjects with Type 2 Diabetes Who Are Not Achieving Glycemic Targets
Type 2 Diabetes Mellitus
Phase 4
No
pramlintide acetate
All
200
Interventional
18 Years - 75 Years
Allocation: Randomized
Endpoint Classification: Safety/Efficacy
Intervention Model: Parallel Assignment
Masking: Double Blind
Primary Purpose: Treatment
Verified 01 Mar 2015 by AstraZeneca Pharmaceuticals
AstraZeneca Pharmaceuticals
N/A
The purpose of this study is to evaluate the efficacy and safety of adding Symlin to an established regimen of insulin glargine in subjects with type 2 diabetes who are not achieving glycemic targets.
Location
Location
Portland, OR, United States
Location
Dallas, TX, United States
Location
Baton Rouge, LA, United States
Location
Washington, DC, United States
Location
Los Gatos, CA, United States
Location
Charlotte, NC, United States
Location
Durham, NC, United States
Location
Chesterfield, MO, United States
Arms | Assigned Interventions |
---|---|
Active Comparator: Pramlintide | Drug: pramlintide acetate Clear, colorless, sterile solution for SC injection |
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