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Semaglutide

Ozempic, Rybelsus, Wegovy

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Studies 78
Trials 100
Completed OBSERVATIONAL NCT06659679

Emulating the PIONEER6 Diabetes Trial Using Healthcare Claims

View on ClinicalTrials.gov Updated Dec 15, 2025

Brief Summary

Investigators are building an empirical evidence base for real world data through large-scale emulation of randomized controlled trials. The investigators' goal is to understand for what types of clinical questions real world data analyses can be conducted with confidence and how to implement such studies.

Detailed Description

This is a non-randomized, non-interventional study that is part of the RCT DUPLICATE initiative (www.rctduplicate.org) of the Brigham and Women's Hospital, Harvard Medical School. It is intended to emulate, as closely as is possible in healthcare insurance claims data, the trial listed below/above. Although many features of the trial cannot be directly emulated in healthcare claims, key design features, including outcomes, exposures, and inclusion/exclusion criteria, were selected to proxy those features from the trial. Randomization is also not emulable in healthcare claims data but was proxied through a statistical balancing of measured covariates according to standard practice. Investigators assume that the RCT provides the reference standard treatment effect estimate and that failure to replicate RCT findings is indicative of the inadequacy of the healthcare claims data for emulation for a range of possible reasons and does not provide information on the validity of the original RCT finding. The PIONEER6 trial, is a is a non-inferiority trial to evaluate the effects of oral semaglutide versus placebo in terms of cardiovascular safety (CV death, nonfatal MI, or nonfatal stroke) in patients with type 2 diabetes. The database study designed to emulate PIONEER6 will be a new-user active comparative study, where we compare the effect of oral semaglutide versus sitagliptin on MACE outcome among patients with T2DM. Sitagliptin was selected to act as an active-comparator proxy for placebo. Sitagliptin and the class of dipeptidyl peptidase-4 (DPP-4) inhibitors have been demonstrated not to have an effect on MACE in a series of RCTs, and they are used in similar stages of disease/line of therapy as semaglutide, as well as being similarly costly.

Interventions

Name: New use of oral semaglutide
Type: DRUG
Description: New use of oral semaglutide dispensing claim is used as the exposure.
Name: New initiation of sitagliptin
Type: DRUG
Description: New use of sitagliptin dispensing claim is used as the reference.

Primary Outcomes

Measure: Major adverse cardiac event (MACE), including myocardial infarction, stroke, and all cause death
TimeFrame: Through study completion (1 day after cohort entry date until the first of outcome or censoring)
Description: Hazard ratio

Trial Information

NCT ID

NCT06659679

Status

Completed

Study Type

OBSERVATIONAL

Sponsor

Brigham and Women's Hospital

Last Updated

December 15, 2025