Cognitive Dysfunction and Glucagon-like Peptide-1 Agonists
NCT02423824 on ClinicalTrials.gov · last registry update 2016-05-13
A small phase 3 — 21 participants, against a typical 424. The sponsor logged completion for April 2016. Primary outcome, as filed: Executive function. liraglutide is approved in the US, but not for psychiatric — a registration here is not an approval, and most drugs tested in a new condition never get one for it.
- Status
- COMPLETED
- Phase
- P3
- Drug
- liraglutideSaxenda, Victoza, Xultophy
- Sponsor type
- Other
- Enrollment
- 21
- Started
- 2015-05
- Primary completion
- 2016-04 actual
Observed history
No changes recorded since monitoring began on 2026-08-21. This record has held steady. If a reporting date moves, a status changes or enrollment is resized, it will appear here with the previous value alongside the new one.
Primary outcome
Executive function
Conditions studied
Bipolar Disorder · Major Depressive Disorder
Every field above is taken directly from the registry record. See all detected changes across the class, or the liraglutide page for this molecule’s full trial and approval history.