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sitagliptin

Generic: SITAGLIPTIN HYDROCHLORIDE·Brand: BRYNOVIN, JANUVIA, Janumet, Januvia, SITAGLIPTIN PHOSPHATE, ZITUVIO

sitagliptin: 4 clinical trials tracked.

sitagliptin evidence translation

What we can confirm

4 tracked trials

No verified listed company relationship

What it means

AI will separate confirmed drug evidence from unknown company context.

What to watch

Watch trial status, endpoints, and the next source-backed update.
BioSniper AIPage evidence connected

Prepared research question

What is verified about sitagliptin, and what remains unknown?

Run cited research

Traceable citations · Unknowns marked

See linked entities and source evidence6 indications · 2 study sponsors
Clinical Trial Registry Records (4)

A Phase 1 Study to Evaluate the Effect of Multiple Doses of ABBV-722 on the Pharmacokinetics of Cocktail Probe Substrates of CYP3A and Select Transporters in Healthy Adult Subjects

NCT07567781Registry updated 2026-08-20·Phase 1·ABBV
Completed

Primary endpoint: Number of Participants with Adverse Events (AEs)

Interventionalopen12 enrolledStarted 2026-04Completion 2026-071 site · United StatesAbbVie

Comparative Effectiveness of Dulaglutide, Semaglutide, and Tirzepatide in Preventing Cardiovascular Events in Patients With Type 2 Diabetes and Obesity With or Without Atherosclerotic Cardiovascular Disease.

NCT07417618Registry updated 2026-02-18·N/A
Active, not recruiting

Primary endpoint: Composite of myocardial infarction, stroke, or all-cause mortality.

Observational60,000 targetStarted 2026-01Completion 2026-031 site · United StatesBrigham and Women's Hospital

The GLP-1 Agonist Semaglutide for the Treatment of Metabolic Disease in Liver Transplant Recipients: A Phase IV, Randomized Trial

NCT05195944Registry updated 2026-04-06·Phase 4
Enrolling by invitation

Primary endpoint: Change in HbA1c level

InterventionalRandomizedquadruple58 targetStarted 2022-10Completion 2026-121 site · CanadaUniversity Health Network, Toronto

Phase 2, Randomized, Double-Blind, Placebo and Active-Comparator Controlled Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of MBX-2982 Administered Daily for 4 Weeks as Monotherapy in Patients With Type 2 Diabetes

NCT01035879Registry updated 2026-09-18·Phase 2·GILD
Completed

Primary endpoint: Evaluate the effect of MBX-2982 on the absolute and percent change from baseline and placebo in mean weighted average of 14-point blood glucose levels associated with a standardized breakfast and lunch

InterventionalRandomizedtriple100 enrolledStarted 2009-12Completion 2010-0814 sites · Georgia, India, United StatesGilead Sciences