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Clinical Trial Summary

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).


Clinical Trial Description

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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06174116
Study type Interventional
Source University of Massachusetts, Worcester
Contact Abaigeal Grant, BA
Phone 5088563027
Email abaigeal.grant2@umassmed.edu
Status Recruiting
Phase Phase 4
Start date April 2, 2024
Completion date November 2026

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