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The main question this study is trying to answer is whether lumateperone, an FDA-approved antipsychotic drug, can help reduce possible side effects of clozapine, such as weight gain and elevated levels of sugar and bad cholesterol. Participants will be randomly assigned to either take lumateperone (Caplyta) or a placebo for 12 weeks, in addition to their regularly prescribed clozapine. During their participation, patients will answer questions about their psychiatric and daily functioning, have blood drawn, and have their body composition analyzed (similar to stepping on a scale).
This is a 12-week study in which we investigate how adjunctive lumateperone affects lipid particle size and body composition in clozapine-treated patients with schizophrenia; in addition, we will investigate if lumateperone improves insomnia. Outcome measures will record a variety of assessments related to participants' psychiatric symptoms, psychosocial functioning, and biological outcomes.
Age
18 - 65 years
Sex
ALL
Healthy Volunteers
No
UMass Chan Medical School
Worcester, Massachusetts, United States
Start Date
April 2, 2024
Primary Completion Date
August 1, 2026
Completion Date
November 1, 2026
Last Updated
May 20, 2025
50
ESTIMATED participants
Lumateperone
DRUG
Placebo
DRUG
Lead Sponsor
University of Massachusetts, Worcester
Collaborators
NCT07455929
NCT06740383
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
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