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An Exploratory Analysis of Immune and Inflammatory Response Associated With Clozapine

Primary Purpose

Treatment-resistant Schizophrenia

Status
Recruiting
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
Clozapine
Antipsychotics,Other (non-Clozapine)
Sponsored by
Ohio State University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Treatment-resistant Schizophrenia

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: All participants: Between 18 and 65 years of age Physically healthy (no clinically significant unstable medical condition as confirmed by medical history and physical examination) Able to give informed consent Treatment-Refractory Schizophrenia Clozapine treatment group (n = 30) Individuals treated with Clozapine consistently for a minimum of 6 months Non-Clozapine treatment group Continued treatment with non-Clozapine antipsychotic but would be eligible for Clozapine with the provider/patient electing to not pursue such for clinical reasons, consistently treated for at least 6 months Exclusion Criteria: Clinically significant medical condition; cardiovascular, pulmonary, endocrine, or renal condition requiring in depth medical treatment Active or recent (within 4 weeks) bacterial or viral infection Chronic viral infection (hepatitis, HIV) History of autoimmune, or chronic inflammatory condition Current treatment with lithium Treatment with Clozapine in the past 6 months Current treatment with immunomodulatory or anti-inflammatory therapy Vaccination within the past 3 months Current alcohol or substance use disorder of moderate or severe severity Intellectual disability (i.e. intelligence quotient <70) Unwilling or unable to sign informed consent document Pregnancy Any patient deemed ineligible by PI discretion

Sites / Locations

  • Ohio State University Harding HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Clozapine Arm

Non-Clozapine arm

Arm Description

Patients will be on Clozapine for at least 6 months

Patients will be on non-Clozapine antipsychotic for at least 6 months

Outcomes

Primary Outcome Measures

Interleukin-6 (IL-6)
Comparison in interleukin-6 between Clozapine and non-Clozapine group

Secondary Outcome Measures

Other immune/cardiac markers
Comparison in hsCRP, interleukin-1β, interferon-γ, transforming growth factor-β, tumor necrosis factor between Clozapine and non-Clozapine group
Positive and Negative Syndrome symptom Scale
Comparison in psychosis rating scales (PANSS) between Clozapine and non-Clozapine group. Higher scores indicate more severe symptoms of psychosis. Score from 30-210
Self-injurious Thoughts and Behaviors Interviews
Comparison between Clozapine and non-Clozapine group in Suicidality rating scales. Scores on rating will be binary (yes/no) for suicidal ideation and also suicide attempts.

Full Information

First Posted
January 20, 2023
Last Updated
October 4, 2023
Sponsor
Ohio State University
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1. Study Identification

Unique Protocol Identification Number
NCT05741502
Brief Title
An Exploratory Analysis of Immune and Inflammatory Response Associated With Clozapine
Official Title
An Exploratory Analysis of Immune and Inflammatory Response Associated With Clozapine Versus Non-Clozapine Antipsychotics in Individuals With Treatment-resistant Schizophrenia
Study Type
Interventional

2. Study Status

Record Verification Date
October 2023
Overall Recruitment Status
Recruiting
Study Start Date
August 16, 2023 (Actual)
Primary Completion Date
March 2026 (Anticipated)
Study Completion Date
June 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Ohio State University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
Yes
Studies a U.S. FDA-regulated Device Product
No
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
The specific aim of this protocol is to compare Clozapine treatment vs Non-Clozapine antipsychotic treatment in a population of treatment-refractory individuals with schizophrenia. Specifically, it is to test if Clozapine leads to a decrease in levels of inflammatory markers, namely interleukin-6 but with an exploratory view of other markers. Clozapine has superior efficacy and is the only medication approved for treatment-refractory schizophrenia in addition to decreasing the risk of suicidal behavior as well. It is unclear why Clozapine has increased efficacy from a mechanistic viewpoint. We will look at the role of inflammatory markers and assess them 1x along with rating scales for psychosis and suicidality, the other entities which Clozapine has been shown to improve.
Detailed Description
This study is designed to investigate if treatment with the antipsychotic Clozapine is associated with changes in various immune and inflammatory biomarkers when compared to treatment with non-Clozapine antipsychotic treatments. Clozapine is a uniquely efficacious treatment of psychotic disorders, the only effective agent in approximately 30-40% of individuals with treatment refractory symptoms. Clozapine, unlike other antipsychotic drugs, often precipitates a unique, multi-systemic inflammatory response most widely recognized in the cardiovascular system but also likely the central nervous system (CNS) which is tied into its unique side effect profile but might also account for its increased efficacy. Schizophrenia spectrum disorders affect about 1% of the population with around 30-40% of those diagnosed with symptoms refractory to standard, non-Clozapine antipsychotic treatment. We will measure various inflammatory markers 1x for patients who are stable outpatients. Participants will be patients with treatment-resistant schizophrenia on clozapine treatment for at least 6 months referred from OSU's outpatient clinic with a comparator group also referred from Ohio State University, having shown treatment resistant symptoms but with provider/patient electing not to use clozapine for clinically relevant reasons and have been on antipsychotic medication for at least 6 months. The study includes 1 visit including symptom rating scale assessments and laboratory draw for collection of serum samples and the visit also having more diagnostic assessments to assure proper enrollment. If the study results are positive meaning there is a difference between the two groups, it would help elucidate the potential mechanisms by which Clozapine works and demonstrates increased efficacy for those with treatment-refractory schizophrenia, a severely debilitating, life long illness with marked disability. This would also allow for further studies to explore this mechanism and the role of inflammation and the immune system as well.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Treatment-resistant Schizophrenia

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Model Description
Parallel open-label groups of Treatment-Refractory schizophrenia patients treated with Clozapine or non-Clozapine drug
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Non-Randomized
Enrollment
60 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Clozapine Arm
Arm Type
Experimental
Arm Description
Patients will be on Clozapine for at least 6 months
Arm Title
Non-Clozapine arm
Arm Type
Active Comparator
Arm Description
Patients will be on non-Clozapine antipsychotic for at least 6 months
Intervention Type
Drug
Intervention Name(s)
Clozapine
Intervention Description
We will assess inflammatory/immune marker labs
Intervention Type
Drug
Intervention Name(s)
Antipsychotics,Other (non-Clozapine)
Other Intervention Name(s)
Including Olanzapine, Risperidone, Paliperidone, Quetiapine, Aripiprazole, Ziprasidone, Lurasidone, Cariprazine, and all Typical antipsychotics
Intervention Description
We will assess monitor inflammatory/immune marker lab
Primary Outcome Measure Information:
Title
Interleukin-6 (IL-6)
Description
Comparison in interleukin-6 between Clozapine and non-Clozapine group
Time Frame
Up to 1 year
Secondary Outcome Measure Information:
Title
Other immune/cardiac markers
Description
Comparison in hsCRP, interleukin-1β, interferon-γ, transforming growth factor-β, tumor necrosis factor between Clozapine and non-Clozapine group
Time Frame
Up to 1 year
Title
Positive and Negative Syndrome symptom Scale
Description
Comparison in psychosis rating scales (PANSS) between Clozapine and non-Clozapine group. Higher scores indicate more severe symptoms of psychosis. Score from 30-210
Time Frame
Up to 1 year
Title
Self-injurious Thoughts and Behaviors Interviews
Description
Comparison between Clozapine and non-Clozapine group in Suicidality rating scales. Scores on rating will be binary (yes/no) for suicidal ideation and also suicide attempts.
Time Frame
Up to 1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: All participants: Between 18 and 65 years of age Physically healthy (no clinically significant unstable medical condition as confirmed by medical history and physical examination) Able to give informed consent Treatment-Refractory Schizophrenia Clozapine treatment group (n = 30) Individuals treated with Clozapine consistently for a minimum of 6 months Non-Clozapine treatment group Continued treatment with non-Clozapine antipsychotic but would be eligible for Clozapine with the provider/patient electing to not pursue such for clinical reasons, consistently treated for at least 6 months Exclusion Criteria: Clinically significant medical condition; cardiovascular, pulmonary, endocrine, or renal condition requiring in depth medical treatment Active or recent (within 4 weeks) bacterial or viral infection Chronic viral infection (hepatitis, HIV) History of autoimmune, or chronic inflammatory condition Current treatment with lithium Treatment with Clozapine in the past 6 months Current treatment with immunomodulatory or anti-inflammatory therapy Vaccination within the past 3 months Current alcohol or substance use disorder of moderate or severe severity Intellectual disability (i.e. intelligence quotient <70) Unwilling or unable to sign informed consent document Pregnancy Any patient deemed ineligible by PI discretion
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Walter H Stearns, MD
Phone
6146853221
Email
walter.stearns@osumc.edu
First Name & Middle Initial & Last Name or Official Title & Degree
Craig J Parris, MS
Phone
6146858623
Email
craig.parris@osumc.edu
Facility Information:
Facility Name
Ohio State University Harding Hospital
City
Columbus
State/Province
Ohio
ZIP/Postal Code
43210
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Walter H Stearns, MD
Phone
614-685-3221
Email
walter.stearns@osumc.edu
First Name & Middle Initial & Last Name & Degree
Craig J Parris, MS
Phone
6146858623
Email
craig.parris@osumc.edu

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

An Exploratory Analysis of Immune and Inflammatory Response Associated With Clozapine

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