Economic Outcomes of EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) in T2D Patients Who Are New to Injectable Therapy
Completed
Conditions studied: Diabetes Mellitus Type 2
In brief
Primary objective of this study is to compare diabetes-related healthcare utilization and costs in patients initiating exenatide once weekly vs insulin glargine.
Key facts
- Study ID
- NCT02843399
- Run by
- AstraZeneca
- People needed
- 15498
- Starts
- 2016-08-15
- Expected to finish
- 2016-12-15
- Last updated by the study team
- 2017-12-15
Who can join
Age: 18 and older, up to 99. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- One or more outpatient prescription claim for EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) between February 1, 2012, and June 30, 2014 (date of first claim = index date; medication to which first claim corresponds = index therapy).
- Aged 18 or older as of the index date.
- Continuous enrollment in medical and pharmacy benefits for 12 months before (baseline period) and 12 months after (follow-up period) the index date. (6 months follow-up will be provided to determine the effect on sample size.)
- One or more medical claims with a diagnosis code for T2DM (ICD-9-CM 250.x0 or 250.x2) in the baseline period or on the index date.
You may not qualify if…
- No outpatient prescription claims for any injectable glucose-lowering medication during the baseline period (GLP-1RA or insulins).
- No medical claims with a diagnosis (or procedure, where appropriate) code indicative for type 1 diabetes mellitus (ICD-9-CM 250.x1 or 250.x3), gestational diabetes (ICD-9-CM 648.8x), or pregnancy or childbirth in the baseline or follow-up periods.
Where it is running
- Research site — Wilmington, Delaware, United States
Full record on ClinicalTrials.gov
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