IL-23 Inhibitor for Schizophrenia
What You Need to Know Before You Apply
What is the purpose of this trial?
This trial explores a new treatment approach for individuals with schizophrenia or schizoaffective disorder who have specific immune markers. It tests whether mirikizumab, an FDA-approved drug targeting inflammation, can improve symptoms like lack of pleasure and social withdrawal when added to current antipsychotic medications. Participants must have elevated anti-gliadin antibodies (AGA IgG), which are linked to increased inflammation. The trial aims to provide a targeted treatment for symptoms that standard therapies struggle to manage. Individuals with schizophrenia who have tested positive for AGA IgG antibodies may find this trial suitable. As a Phase 4 trial, it focuses on understanding how this already FDA-approved and effective treatment can benefit more patients.
Will I have to stop taking my current medications?
You can continue taking your current antipsychotic medications, but you cannot take immunosuppressive or certain anti-inflammatory medications like NSAIDs or high-dose aspirin. If you use anti-inflammatory medications occasionally, that's allowed.
What is the safety track record for mirikizumab?
Research has shown that mirikizumab, the treatment under study in this trial, is generally well-tolerated. In one study involving patients with ulcerative colitis, 7.4% of those taking mirikizumab experienced serious side effects, which are important but not very common. Additionally, 5.3% of patients discontinued the treatment due to these side effects. Most reported side effects were mild. These findings suggest that while some risks exist, mirikizumab is generally safe for use in other conditions, indicating a positive safety profile for this trial.12345
Why are researchers enthusiastic about this study treatment?
Unlike the standard antipsychotics for schizophrenia, which typically target dopamine receptors, Mirikizumab offers a fresh approach by focusing on the IL-23 pathway. This is significant because IL-23 is linked to immune system regulation and inflammation, which recent research suggests might play a role in schizophrenia. Researchers are excited about Mirikizumab's potential to address untreated aspects of the disorder, possibly leading to a more comprehensive treatment with fewer side effects associated with current options.
What evidence suggests that mirikizumab could be an effective treatment for schizophrenia?
This trial will compare the effects of mirikizumab, an IL-23 inhibitor, with a placebo in patients with schizophrenia. Studies have shown that mirikizumab, which blocks a specific protein involved in inflammation, effectively treats conditions with immune-related inflammation. In patients with ulcerative colitis, 24.2% of participants in a study experienced significant symptom relief by week 12. This suggests that mirikizumab can reduce inflammation and improve health outcomes. While primarily used for ulcerative colitis, it might also benefit a subgroup of schizophrenia patients with high inflammation levels. Early research indicates that targeting this immune pathway could offer new hope for treating symptoms like lack of motivation and thinking difficulties in these patients.12367
Who Is on the Research Team?
Deanna L Kelly, PharmD, BCPP
Principal Investigator
University of Maryland, Baltimore
Are You a Good Fit for This Trial?
This trial is for people with schizophrenia or schizoaffective disorder who test positive for a specific immune marker (AGA IgG antibodies). Healthy volunteers may also be included as controls. Participants must meet screening requirements and not have conditions that would make participation unsafe.Inclusion Criteria
Exclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive mirikizumab or placebo for 16 weeks to assess changes in negative symptoms and cognitive impairments
Follow-up
Participants are monitored for safety and effectiveness after treatment
What Are the Treatments Tested in This Trial?
Interventions
- Mirikizumab
Trial Overview
The study tests mirikizumab, an IL-23 inhibitor, versus placebo in addition to usual antipsychotic treatment over 16 weeks. It focuses on whether this drug can improve negative symptoms and thinking problems in a subgroup of patients identified by their immune status.
How Is the Trial Designed?
2
Treatment groups
Active Control
Placebo Group
Find a Clinic Near You
Who Is Running the Clinical Trial?
University of Maryland, Baltimore
Lead Sponsor
Citations
Safety and efficacy of IL-23 inhibitors in patients with moderate ...
According to Sandborn et al., mirikizumab showed clinical efficacy in adults with moderate to severe UC, with remission achieved in 24.2% of patients by week 12 ...
Clinical Trial of an IL-23 Inhibitor for Immune Activation in ...
This 16 week clinical trial investigates a precision-medicine approach to schizophrenia by targeting a biologically distinct subgroup,- ...
Efficacy and Safety of IL-23 Inhibitors in the Treatment ...
Mirikizumab demonstrates a significant reduction in cardiological consequences, with a log risk ratio of -1.36 (95% CI: -1.93 to -0.80).
Lilly's mirikizumab is first and only IL23p19 antagonist to ...
Among patients receiving mirikizumab in the LUCENT-3 study, 7.4% of patients reported a serious adverse event (AE), while 5.3% discontinued ...
5.
gastroenterologyadvisor.com
gastroenterologyadvisor.com/cch/ulcerative-colitis-remission-efficacy-safety-lucent-3-mirikizumab/Long-Term Efficacy and Safety of Mirikizumab for ...
Clinical remission rates for these week 52 responders were recorded at 56%, while corticosteroid-free (CSF) remission was 55%. Additionally, endoscopic ...
Study Details | NCT07059130 | Evaluating the Efficacy and ...
This research study looks at how safe and effective a medicine called Mirikizumab is for treating older adults (aged 60 and above) who have moderate to severe ...
7.
scholars.mssm.edu
scholars.mssm.edu/en/publications/three-year-efficacy-and-safety-of-mirikizumab-following-152-weeksThree-Year Efficacy and Safety of Mirikizumab Following 152 ...
Efficacy and safety outcomes are reported for mirikizumab-treated LUCENT-3 participants, including biologic-failed patients, with data for ...
Unbiased Results
We believe in providing patients with all the options.
Your Data Stays Your Data
We only share your information with the clinical trials you're trying to access.
Verified Trials Only
All of our trials are run by licensed doctors, researchers, and healthcare companies.