Status: Not yet recruiting
Lumateperone for Late-Life Depression
The purpose of this research study is to examine how well a medication called lumateperone (Caplyta) works to relieve depression in older adults with treatment-resistant depression. Lumateperone (Caplyta) is approved by the U.S. Food and Drug Administration to treat Major Depressive Disorder in adults who are also taking another antidepressant medication. This study will compare lumateperone (Caplyta) to placebo (a sugar pill without medication).
Participants needed: 100
Trial details
Phase: Phase 3Age: 60+Biological sex: AllType: InterventionalSponsor: Eric LenzeUpdated: Jun 3, 2026Locations: 2
Eligibility criteria
Age >=60 [+5]
Dementia [+3]