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CompletedResults posted

Comparison of Type 2 Diabetes Pharmacotherapy Regimens

Comparison of Type 2 Diabetes Pharmacotherapy Regimens Using Targeted Learning

Lead sponsor

Kaiser Permanente

Assets

Exenatide / Liraglutide

Listed sites

6

Recruiting sites

-

Actual enrollment

241,981

Study population

Type 2 diabetes

Eligibility highlights

-

Primary endpoint

3-point MACE (Cardiovascular death, Non-fatal MI, Non-fatal stroke)

Registered trial locations

Locations reported to ClinicalTrials.gov for this trial snapshot. Site count is not enrollment count; per-site enrollment is not available from source.

Identifiers

Registered as

NCT IDNCT05073692
Org study ID739857

Timeline

Milestones

Study start2021-07-01actual
Study first posted2021-10-11actual
Primary completion2024-12-31actual
Study completion2025-03-12actual
Last update posted2025-11-21actual
Results first posted2025-11-21actual

Assets

Investigational agents

Who this study enrolls

Type 2 diabetes

Who can enroll

Minimum age18 Years
Maximum age85 Years
SexAll
Healthy volunteersNot accepted
Sampling methodNon probability sample

Study population text

Patients from six large care delivery systems with integrated administrative and EHR clinical data sources (Geisinger in Pennsylvania, Henry Ford Health System in Michigan, HealthPartners Institute in Minnesota and Wisconsin, and Kaiser Permanente of Northern California, Southern California, and Hawaii) who were new users of glucose-lowering medications between 01/01/2014 and 12/31/2021.

Eligibility criteria

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

Endpoints (2)

What's being measured

Protocol endpoints and posted registry outcome measures, grouped into outcome categories. Composite endpoints show their component event types. Standard codes (LOINC, SNOMED CT) are shown where available.

Cardiovascular outcomes

2 endpoints
Primary/registry result

Incidence of 3-point Major Adverse Cardiovascular Events (MACE)

Time frame:2.5 years

3-point MACE

composite event, event

componentsCardiovascular death, Non-fatal MI, Non-fatal stroke

Posted result

GroupParticipants95% CI
SU Initiators11,348-
DPP4 Initiators393-
SGLT2i Initiators424-
GLP-1RA Initiators296-
Primary/protocol endpoint

Incidence of 3-point Major Adverse Cardiovascular Events (MACE)

Time frame:2.5 years

3-point MACE

composite event, event

componentsCardiovascular death, Non-fatal MI, Non-fatal stroke

Publications (4)

Bibliography

Records linked to this trial through ClinicalTrials.gov references, PubMed NCT search, and curated study seeds. 'Canonical' marks design/result papers; others are registry references or candidates.

Provenance

Sources

Trial identity, design, statusClinicalTrials.gov API v2
Snapshot dateJuly 6, 2026
Endpoint classificationDelfa endpoint taxonomy v2 (May 13, 2026)
Results tableClinicalTrials.gov results section

Trial facts come from public ClinicalTrials.gov records. Endpoint categories are Delfa's classification of those records, not a ClinicalTrials.gov field. All figures reflect the July 6, 2026 snapshot.