Metabolic Effects of Adjunctive Lumateperone Treatment in Clozapine-Treated Patients With Schizophrenia

Status: Recruiting
Location: See location...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 4
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).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Meets the DSM-5 criteria for diagnoses of schizophrenia or schizoaffective disorder based on the MINI International Neuropsychiatric Interview (MINI 7.0)

• On clozapine treatment for at least 6 months

• Stable dose of antipsychotic treatment for at least 1 month

• Well established compliance with outpatient medications

• Subjects of child-bearing potential are required to practice appropriate birth control methods during the study.

Locations
United States
Massachusetts
UMass Chan Medical School
RECRUITING
Worcester
Contact Information
Primary
Abaigeal Grant, BA
abaigeal.grant2@umassmed.edu
5088563027
Time Frame
Start Date: 2024-04-02
Estimated Completion Date: 2026-11
Participants
Target number of participants: 50
Treatments
Placebo_comparator: Placebo
2 Placebo capsules taken orally per day for 12 weeks
Experimental: Lumateperone
42mg (two 21mg capsules) lumateperone (Caplyta) taken orally per day for 12 weeks
Related Therapeutic Areas
Sponsors
Leads: University of Massachusetts, Worcester
Collaborators: Intra-Cellular Therapies, Inc.

This content was sourced from clinicaltrials.gov