Schizophrenia Clinical Trials
83 studies are recruiting for schizophrenia in the United States right now. Each one is listed on ClinicalTrials.gov, the public registry the research teams themselves file with. TrialBoost is not a doctor, a research site, or a study sponsor: the research team decides who takes part.
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Studies now recruiting
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A Study to Evaluate the Effectiveness of Valbenazine in Adult Participants With Tardive Dyskinesia (TD) Who Remain Symptomatic While Receiving or After Stopping a Vesicular Monoamine Transporter 2 (VMAT2) Inhibitor
This study will evaluate the efficacy of valbenazine on clinician- and patient-reported outcomes in participants with TD while receiving or after stopping a VMAT2 inhibitor.
- Stage
- Phase 4
- Ages
- 18 and older
- Site
- Neurocrine Clinical Site, Bryant, Arkansas
- Locations
- 19 in total
- Run by
- Neurocrine Biosciences
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A Study of LTX-001 In Adult Participants With Acute Exacerbation of Schizophrenia
The purpose of this clinical trial is to learn whether the investigational drug LTX-001 is safe and well tolerated in adults with a diagnosis of schizophrenia who are having a recent worsening of their symptoms (an acute exacerbation). Additional questions it aims to answer are: * how does the amou…
- Stage
- Phase 1
- Ages
- 18 to 55
- Site
- Pillar Clinical Research, LLC, Little Rock, Arkansas
- Locations
- 10 in total
- Run by
- Leal Therapeutics, Inc
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Circuitry-Guided Smoking Cessation in Schizophrenia (UH3)
Patients with schizophrenia spectrum disorder (SSD) will be exposed to active repetitive transcranial magnetic stimulation (rTMS) from F8 coil or active rTMS from H coil for smoking cessation. Smoking and brain functional connectivity changes will be assessed at baseline, different stages of rTMS a…
- Stage
- Not phased
- Ages
- 22 to 65
- Site
- The University of Texas Health Science Center, Houston, Houston, Texas
- Run by
- The University of Texas Health Science Center, Houston
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A Study to Assess Adverse Events, Change in Disease Activity, and How Oral Emraclidine Moves Through the Body in Adult Participants With Schizophrenia
Schizophrenia is a common and severe psychiatric illness characterized by extreme disturbances of cognition and thought, affecting language, perception and sense of self. This study will assess adverse events, change in disease activity, and how oral emraclidine moves through the body in adult part…
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- Woodland International Research Group /ID# 275747, Little Rock, Arkansas
- Locations
- 7 in total
- Run by
- AbbVie
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Relapse Prevention Trial Evaluating KarXT Treatment in Schizophrenia
The purpose of the study is to evaluate the relapse prevention of KarXT in the treatment of participants with Schizophrenia
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Pillar Clinical Research - Bentonville, Bentonville, Arkansas
- Locations
- 59 in total
- Run by
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
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52-week Open Label Safety-Tolerability Study
Phase 3, open label, multicenter study designed to assess the long term safety and tolerability of LB-102 for the treatment of adult patients with stable schizophrenia
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Chandler Clinical Trials, Chandler, Arizona
- Locations
- 23 in total
- Run by
- LB Pharmaceuticals Inc.
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A Study to Evaluate the Efficacy and Safety of KarXT for the Treatment of Schizophrenia in Adolescents (EMERGENT TEEN)
The purpose of this study is to evaluate the efficacy and safety of KarXT for treatment of Schizophrenia in adolescents.
- Stage
- Phase 3
- Ages
- 13 to 17
- Site
- Advanced Research Center Inc., Anaheim, California
- Locations
- 38 in total
- Run by
- Bristol-Myers Squibb
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A Study of Brenipatide in Adult Participants With Schizophrenia
The purpose of this study is to assess the efficacy and safety of brenipatide when administered with standard of care (SoC) compared to placebo plus SoC for treatment of schizophrenia. The trial is divided into three periods as follows: Screening period will last approximately 1 month, treatment pe…
- Stage
- Phase 2
- Ages
- 18 to 55
- Site
- Pillar Clinical Research- Little Rock, Little Rock, Arkansas
- Locations
- 103 in total
- Run by
- Eli Lilly and Company
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Genetic Basis of the Risk and Consequences of Cannabis Exposure in Humans
Cannabis is widely used worldwide and is associated with negative outcomes including cannabis use disorder (CanUD), psychosis, and cognitive impairment amongst others. Given the legalization of "recreational" and "medical" cannabis globally, the increasing availability of cannabis, the higher poten…
- Stage
- Phase 1
- Ages
- 21 to 60
- Site
- West Haven Veterans Affairs Medical Center, West Haven, Connecticut
- Run by
- Yale University
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A Study to Evaluate the Safety, Tolerability, and PK of an Injectable Form of KarXT
A study to evaluate the safety, tolerability, and PK of an injectable form of KarXT in participants with schizophrenia
- Stage
- Phase 1
- Ages
- 18 to 55
- Site
- Collaborative Neuroscience Research, LLC, Los Alamitos, California
- Locations
- 8 in total
- Run by
- Bristol-Myers Squibb
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A Long-Term Open-Label Study of ML-007C-MA in Adults With Schizophrenia
ML-007C-MA-212 is a 52-week open-label study designed to evaluate the long-term safety, tolerability, and effectiveness of ML-007C-MA in participants with schizophrenia who have recently completed an antecedent study (ML-007C-MA-211) or enroll directly (De Novo Cohort).
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- Clinical Site, Little Rock, Arkansas
- Locations
- 42 in total
- Run by
- MapLight Therapeutics
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Overnight Thalamic TES-TI to Modulate Sleep Spindles in Individuals With Schizophrenia Spectrum Disorders and Matched Healthy Controls
This study to find out whether a type of non-invasive electrical brain stimulation called transcranial electrical stimulation with temporal interference (TES-TI) can temporarily change brain activity during sleep-especially sleep spindles (brain rhythms in the ~8-16 Hz range). The investigators are…
- Stage
- Not phased
- Ages
- 18 to 50
- Site
- University of Wisconsin, Madison, Wisconsin
- Run by
- University of Wisconsin, Madison
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Safety and Tolerability Trial of Lumateperone in Pediatric Patients With Schizophrenia, Bipolar Disorder or Autism Spectrum Disorder
This is a multicenter, global, 26-week, open-label study to assess the safety and tolerability of lumateperone in pediatric patients with schizophrenia, bipolar disorder or autism spectrum disorder.
- Stage
- Phase 3
- Ages
- 5 to 17
- Site
- Southwest Autism Research and Resource Center, Phoenix, Arizona
- Locations
- 64 in total
- Run by
- Intra-Cellular Therapies, Inc.
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A Study to Evaluate the Long-term Safety and Tolerability of KarXT and KarX-EC for the Treatment of Schizophrenia and Autism-Related Irritability in Adolescents, Respectively
The purpose of this study is to evaluate the long-term safety and tolerability of KarXT and KarX-EC for the treatment of Schizophrenia and autism-related irritability in adolescents, respectively
- Stage
- Phase 3
- Ages
- 5 to 17
- Site
- Advanced Research Center Inc., Anaheim, California
- Locations
- 91 in total
- Run by
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
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A Study of the Feasibility, Safety and Tolerability of Aticaprant as Adjunctive Treatment in Participants With Schizophrenia
The purpose of this study is to see how feasible it is to enroll participants with schizophrenia and for them to complete the study/assessments. It will also assess how safe and tolerable aticaprant is when compared with placebo in participants with schizophrenia.
- Stage
- Phase 1
- Ages
- 18 to 55
- Site
- CNS Network, Garden Grove, California
- Locations
- 8 in total
- Run by
- Janssen Research & Development, LLC
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Study to Evaluate the Safety and Efficacy of Ublituximab in Participants With Schizophrenia
The main objective of this Phase 2 study is to assess the efficacy of ublituximab as measured by Positive and Negative Syndrome Scale (PANSS) total score in participants with schizophrenia.
- Stage
- Phase 2
- Ages
- 18 to 60
- Site
- TG Therapeutics Investigational Trial Site, Little Rock, Arkansas
- Locations
- 2 in total
- Run by
- TG Therapeutics, Inc.
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Cerebellar Modulation of Cognition in Psychosis
The goal of this clinical trial is to learn about cognition in psychotic disorders (schizophrenia, bipolar disorder, and schizoaffective disorder). The main question it aims to answer is: Can we use magnetic stimulation to change processing speed (how quickly people can solve challenging tasks). Pa…
- Stage
- Not phased
- Ages
- 18 to 55
- Site
- McLean Hospital, Belmont, Massachusetts
- Locations
- 2 in total
- Run by
- Mclean Hospital
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Enhancing Veteran-Clinical Collaboration in VA PRRCs
Over 60% of Veterans with serious mental illness have a service-connected disability that impairs their ability to work, go to school, and/or have successful personal lives. Although traditional treatments tend to focus on symptom remission, Veterans prioritize a range of treatment goals, including…
- Stage
- Not phased
- Ages
- 18 and older
- Site
- New Mexico VA Health Care System, Albuquerque, NM, Albuquerque, New Mexico
- Locations
- 3 in total
- Run by
- VA Office of Research and Development
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Evaluation of Treatment Satisfaction and KarXT Utilization Registry (RESKU)
The purpose of this study is to understand treatment preference and satisfaction among adults with schizophrenia in the United States who are prescribed xanomeline and trospium chloride (X/T) therapy
- Stage
- Not phased
- Ages
- 18 and older
- Site
- ATP Clinical Research, Costa Mesa, California
- Locations
- 20 in total
- Run by
- Bristol-Myers Squibb
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Effectiveness and Adverse-effect Switch Evaluation of Xanomeline and Trospium Chloride (KarXT)
The purpose of this study is to describe real-world treatment patterns, effectiveness and adverse events of adults diagnosed with schizophrenia that have initiated xanomeline and trospium chloride (KarXT) treatment in the United States
- Stage
- Not phased
- Ages
- 18 and older
- Site
- SanRo Clinical Research Group, Bryant, Arkansas
- Locations
- 55 in total
- Run by
- Bristol-Myers Squibb
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REACH Study (Recovery Environments: Assessing Cognitive & Brain Health in Community Mental Health)
The purpose of this study is to understand how different types of community-based mental health care affect thinking abilities, daily functioning, and brain activity in adults with schizophrenia and related conditions. The investigators are especially interested in learning whether the Clubhouse Mo…
- Stage
- Not phased
- Ages
- 18 to 50
- Site
- Case Western Reserve University, Cleveland, Ohio
- Run by
- Case Western Reserve University
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Study to Evaluate Weight Gain as Assessed by Change in BMI Z-score in Pediatric Subjects With Schizophrenia or Bipolar I Disorder
To compare changes in body mass index (BMI) Z-score following treatment with OLZ/SAM vs olanzapine
- Stage
- Phase 3
- Ages
- 10 to 17
- Site
- Alkermes Investigator Site, Dothan, Alabama
- Locations
- 47 in total
- Run by
- Alkermes, Inc.
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Determining Efficacy and Safety of BXCL501 in Agitation Associated With Pediatric Schizophrenia and Bipolar Disorder
This is a study of the efficacy and safety of BXCL501 in children and adolescents with acute agitation and either bipolar disorder or schizophrenia.
- Stage
- Phase 1
- Ages
- 10 to 17
- Site
- BioXcel Clinical Research Site, Anaheim, California
- Locations
- 5 in total
- Run by
- BioXcel Therapeutics Inc
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Enhancing Prefrontal Oscillations and Working Memory in Early-course Schizophrenia
This study will investigate the effects of intermittent Theta Burst Stimulation (iTBS) on natural oscillatory frequency of the dorsolateral prefrontal cortex (DLPFC) and working memory in early-course schizophrenia (EC-SCZ). Transcranial magnetic stimulation (TMS) will be used to evoke oscillatory …
- Stage
- Not phased
- Ages
- 18 to 40
- Site
- University of Pittsburgh, Pittsburgh, Pennsylvania
- Run by
- Fabio Ferrarelli
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Improving Cognition Through Telehealth Aerobic Exercise and Cognitive Training After a First Schizophrenia Episode
The participants in the study will receive psychiatric treatment at the UCLA Aftercare Research Program. All participants in this 12-month RCT will receive cognitive training. Half of the patients will also be randomly assigned to the aerobic exercise and strength training condition, and the other …
- Stage
- Not phased
- Ages
- 18 to 45
- Site
- UCLA Aftercare Research Program, Los Angeles, California
- Run by
- University of California, Los Angeles
How to read this page. Every study here comes from ClinicalTrials.gov, the public registry that research teams are required to file with. We have summarised each one in plain language and shown where it is running. We have not changed what any study says it is doing.
What TrialBoost is. We help people find research that might suit them, and, if they ask us to, we pass their details to the research team running it. We are not a doctor, a research site, or a study sponsor, and we do not decide who takes part in anything. Joining costs nothing and you can change your mind at any point.
Paid placement. Some studies pay us when someone asks to be connected to them. Those are labelled Sponsored wherever they appear, and they only appear when they match what you were actually looking for.