DRUG
SU
Exposure to the class of drugs known as Sulfonylureas (SU)
Status
Completed
Phase
Not applicable
Enrollment
241,981
Locations
6
Results
Posted
Publications
4
Study summary
This study is designed to help patients with type 2 diabetes and their clinicians: (a) identify which glucose lowering medications have the most favorable effects on heart health and other patient-important outcomes, (b) inform the timing of medication initiation, and (c) identify whether medication benefits apply equally to all adults with type 2 diabetes, or may be different based on age, sex, race/ethnicity, baseline heart health status, baseline renal function, or other factors.
The study will conduct head-to-head comparisons of type 2 diabetes mellitus (T2DM) treatment strategies using observational data from real-world clinical settings to assess cardiovascular disease (CVD) outcomes and other patient-centered outcomes in T2DM patients with moderate baseline CVD risk who are treated with each of these four classes of glucose-lowering medications known as SGLT2, GLP-1RA, DPP4, and SU. To mitigate bias concerns related to confounding and informative loss to follow-up, analyses will be based on modern causal inference methods combined with machine learning that emulate intention-to-treat (ITT) and per-protocol (PP) analyses of pragmatic randomized trials with active comparators to provide the most robust and precise estimates of relative and absolute effects we would expect in usual care settings. Specific Aims and Hypotheses: Aim 1. Compare the effect off SGLT21, GLP-1RA, DPP4, and SU on each study outcome in adults with T2DM when each type of medication is (a) initiated as second-line therapy after metformin, and (b) initiated as first-, second-, or third-line therapy, or after any history of glucose-lowering therapy independent of prior metformin use. Aim 2. Compare the effect on each study outcome of earlier versus later initiation of SGLT2i, GLP-1RA, DPP4, SU as first-, or second-, or third-line therapy, or after any history of glucose-lowering therapy triggered by various changes in A1C, or CVD risk, or other patient characteristics. Aim 3. Assess in each of the prior analyses whether the treatment effects on study outcomes vary across categories of baseline CVD risk and CVD event history, renal function, congestive heart failure status, age, sex and race/ethnicity, or other patient characteristics. Glucose-lowering medications will be compared at both the class and agent level. The key outcomes that will be considered are MACE 3-point, Myocardial Infarction, Stroke, Heart Failure, Hospitalization, Coronary or Carotid Artery Stent or Bypass Procedure, CVD Mortality, Overall Mortality. Additional patient-centered outcomes will be specified based on insights from stakeholder members of the research team.
Interventions
DRUG
Exposure to the class of drugs known as Sulfonylureas (SU)
DRUG
Exposure to the class of drugs known as Dipeptidyl peptidase-4 inhibitors (DPP4)
DRUG
Exposure to the class of drugs known as Sodium-glucose cotransporter-2 inhibitors (SGLT2i)
DRUG
Exposure to the class of drugs known as Glucagon-like peptide-1 receptor agonists (GLP-1RA)
DRUG
Exposure to either SGLT2i or GLP-1RA
DRUG
Exposure to agent Linagliptin (DPP4)
DRUG
Exposure to agent Exenatide (GLP1-RA)
DRUG
Exposure to agent Liraglutide (GLP-1RA)
DRUG
Exposure to agent Empagliflozin (SGLT2i)
DRUG
Exposure to agent Glimepiride (SU)
DRUG
Exposure to Glimepiride (SU)
DRUG
Exposure to agent Glimepiride (SU) or Glipizide (SU)
Timeline
First posted
Oct 11, 2021
Study start
Jul 1, 2021
Primary completion
Dec 31, 2024
Study completion
Mar 12, 2025
Results posted
Nov 21, 2025
Registry updated
Nov 21, 2025
Outcomes
Incidence of 3-point Major Adverse Cardiovascular Events (MACE)
Time frame · 2.5 years
3-point MACE is defined as a single outcome measure, which is a composite measure of nonfatal myocardial infarction, nonfatal stroke, or cardiovascular disease death.
Not reported in the indexed record.
Eligibility
* Dispensing of either of the set of drugs being compared * No prior dispensing of nor contraindication for any of the drugs compared * Evidence of Type 2 Diabetes Mellitus diagnosis * Age 18 or older * Not currently pregnant * No evidence of dementia or short-term life expectancy from prior cancer diagnoses * History of ≥2 years of continuous health plan membership * ≥1 A1c test in the past 18 months
Study locations
United States. Showing up to 24 locations stored in the fast local snapshot.
Kaiser Permanente Southern California
Pasadena, California, United States
Romain S. Neugebauer
Pleasanton, California, United States
Kaiser Permanente Hawaii
Honolulu, Hawaii, United States
Henry Ford Health System
Detroit, Michigan, United States
HealthPartners Institute
Bloomington, Minnesota, United States
Geisinger
Danville, Pennsylvania, United States
Publications
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Related PeptideStat pages
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