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NCT07824206Not yet recruitingPhase 4

Lumateperone Added to Antidepressant Therapy in Adults With Major Depressive Disorder Experiencing Emotional Blunting

Source: ClinicalTrials.gov · Last updated 17 Sept 2026

Brief summary (registry, in English)

The purpose of this study is to evaluate whether or not adding lumateparone to current antidepressant treatment in adults with major depressive disorder experiencing blunted emotion will reduce or eliminate the blunted emotion as rated by the Oxford Depression Questionnaire.

Status (registry)
Not yet recruiting
Phase (registry)
Phase 4
Study type
Interventional
Enrollment
30 (estimated)
First submitted
11 Sept 2026
Start date
Sept 2026
Primary completion date
Jan 2028
Lead sponsor
Future Options Research, LLC
Diseases
Depression
NCT number
NCT07824206

What you commit to

  • Study type: Interventional · Phase 4
  • Planned participants: 30
  • From Sept 2026 to the primary completion date, Jan 2028
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • \-

Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Future Options Research
Coordinator of this site? Confirm its status
State CollegeUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.