Semaglutide

NCT05768945 trial results

Data Analysis for Drug Repurposing for Effective Alzheimer's Medicines (DREAM)- Semaglutide v DPP4 Inhibitors

Participants
742,670
Status
completed
Completed
2023-12-31
Sponsor
Brigham and Women's Hospital

As posted on ClinicalTrials.gov (NCT05768945), updated at source Nov 10, 2025. Read again whenever the registry updates it. Registry figures can differ from a published paper, which may use another analysis.

Primary outcome

What NCT05768945 measured first

Time to Dementia OnsetIncidence rate per 1000 person year · Median follow up times: 1) 98 days (exp), 134 days (ref) 2) 118 days (exp), 132 days (ref) 3) 90 days (exp), 308 days (ref) 4) 99 days (exp), 135 days (ref) · number
MeasureSemaglutiden=7,129DPP4 Inhibitorsn=7,129
Analysis 14.40(2.27 to 7.68)6.06(3.70 to 9.36)
Analysis 24.69(1.28 to 12.02)6.71(2.70 to 13.83)
Analysis 32.80(0.34 to 10.13)10.24(6.96 to 14.54)
Analysis 40.37(0.01 to 2.04)0.61(0.07 to 2.19)
The trial

How NCT05768945 was run

This study aims to evaluate the comparative risk of dementia/Alzheimer's disease onset between patients treated with medications that target specific metabolic pathways and patients treated with alternative medications for the same indication.

  • Semaglutide: Exposure group
  • DPP4 inhibitors (sitagliptin, saxagliptin, linagliptin, and alogliptin): Reference group
Who could join the trial

Please see https://drive.google.com/drive/folders/1VRjPaaelXFyBbA5gV6pwB\_ijSIMyIJ4N?usp=share\_link or Appendix A(https://drive.google.com/drive/folders/1OgKQlxsJi9UWRDd3Kbaux\_8adngoSnZY?usp=sharing) for full code and algorithm definitions. Medicare timeframe: 2008 to 2019 (end of data availability). Inclusion Criteria: * 1\. Aged \>/= 65 years on the index date * 2\. Enrollment in Medicare Part A, B, and D with no HMO coverage for 365 days prior to and including cohort entry date * 3\. Diagnosis code for type 2 diabetes measured 365 days prior to drug initiation Exclusion Criteria: * 1\. Prior history of dementia measured anytime prior to cohort entry date * 2\. Prior history of nursing home admission in the 365 days prior to the cohort entry date * 3\. Prior use of any GLP receptor agonists (semaglutide, exenatide, liraglutide, albiglutide, dulaglutide, lixisenatide) or DPP4 inhibitors * 4\. Prior use of Semaglutide or DPP4 inhibitors concomitantly on index date

Trial averages do not predict what one person will experience. Results are shown as the registry posts them, without interpretation.

GLPcompare is an informational data platform, not a medical provider or pharmacy. Nothing here is medical advice, a diagnosis, or a recommendation to start, stop, or change any treatment. Data is aggregated from public sources and can be incomplete or out of date. Always confirm with a licensed clinician and the current FDA label.