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| Name | Class |
|---|---|
| Truven health | UNKNOWN |
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Primary objective of this study is to compare diabetes-related healthcare utilization and costs in patients initiating exenatide once weekly vs insulin glargine.
This retrospective, observational cohort analysis will assess medical and pharmacy claims for adult patients with type 2 diabetes from the Truven Health MarketScan® Commercial and Medicare Supplemental claims databases between 2011 and 2015. Diabetes-related healthcare utilization and costs will be measured as a primary outcome. Secondary outcomes include all-cause healthcare utilization and costs, major adverse cardiovascular event (MACE)-related utilization and costs, and medically attended hypoglycemia events.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Exenatide once weekly (EQW) | EQW cohort includes patients with one or more outpatient prescription claims for EQW between 2012 and 2015. | ||
| Insulin Glargine (IG) | IG cohort includes patients with one or more outpatient prescription claims for IG between 2012 and 2015 |
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| Measure | Description | Time Frame |
|---|---|---|
| Diabetes-related HCRU/costs | Compare diabetes-related healthcare utilization and costs in patients initiating EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) | Up to 12 months |
| Measure | Description | Time Frame |
|---|---|---|
| Overall HCRU/Costs | To compare overall healthcare utilization and costs in patients initiating EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) | Up to 12 Months |
| MACE-related HCRU/Costs | To compare major adverse cardiovascular event (MACE)-related healthcare utilization and costs in patients initiating EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) |
| Measure | Description | Time Frame |
|---|---|---|
| Composite of A1C <7%/no weight gain/no hypoglycemia | The exploratory objective of this analysis is to compare attainment of a composite endpoint, and attainment of each of the individual components thereof separately, comprising an HbA1c less than 7%, no weight gain, and no hypoglycemia in patients initiating EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine). This will be conducted among a subset of patients with available laboratory data. |
Inclusion Criteria:
Exclusion Criteria:
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Commercial Insurance
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| Name | Affiliation | Role |
|---|---|---|
| Eric T. Wittbrodt, PharmD, MPH | AstraZeneca | Study Director |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Research site | Wilmington | Delaware | United States |
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| Label | URL |
|---|---|
| Synopsis\_D5551R00012 | View source |
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| ID | Term |
|---|---|
| D003924 | Diabetes Mellitus, Type 2 |
| ID | Term |
|---|---|
| D003920 | Diabetes Mellitus |
| D044882 | Glucose Metabolism Disorders |
| D008659 | Metabolic Diseases |
| D009750 | Nutritional and Metabolic Diseases |
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| Up to 12 Months |
| Medical Hypoglycemic events | To compare rates and costs of medically attended hypoglycemia in patients initiating EQW (Exenatide Once Weekly) vs. IG (Insulin Glargine) | Up to 12 Months |
| Up to 12 Months |
| D004700 | Endocrine System Diseases |