Schizophrenia Clinical Trials
81 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.
Search these by distance from you
By city
Studies now recruiting
-
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
- 68 in total
- Run by
- Bristol-Myers Squibb
-
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.
-
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
- 54 in total
- Run by
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
-
Impact of Cerebellar TMS on Brain and Cognitive Functions in Schizophrenia: a Pilot Study
This is a single-site, sham-controlled, randomized trial in a total of 40 subjects between ages 18 and 60 years with schizophrenia. This study will investigate the effects of 4-week rTMS treatment on brain and cognitive functions in patients. Subjects will be randomized to one of the following arms…
- Stage
- Not phased
- Ages
- 18 to 60
- Site
- Zucker Hillside Hospital, New York, New York
- Run by
- Northwell Health
-
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 60
- Site
- CNS Network, Garden Grove, California
- Locations
- 8 in total
- Run by
- Janssen Research & Development, LLC
-
The Effects of Auditory Stimulation During Sleep on Brain Networks in Schizophrenia
In this research study the investigators will use sleep headbands to measure brain rhythms and to improve their coordination across brain regions. The headbands will be worn at home for multiple nights. On some nights the headbands will play soft sounds at specific times during sleep. The investiga…
- Stage
- Not phased
- Ages
- 18 to 45
- Site
- Massachusetts General Hospital, Charlestown, Massachusetts
- Run by
- Massachusetts General Hospital
-
A Study to Evaluate the Effect of KarXT on Urological Safety
The purpose of this study is to characterize the effect of KarXT on voiding dynamics and urological safety in participants with DSM-5 schizophrenia.
- Stage
- Phase 4
- Ages
- 18 to 65
- Site
- Pillar Clinical Research- Little Rock, Little Rock, Arkansas
- Locations
- 16 in total
- Run by
- Bristol-Myers Squibb
-
A Study to Evaluate the Long-term Safety and Tolerability of Xanomeline and Trospium Chloride for the Treatment of Psychiatric Disorders in Children and Adolescents
The purpose of this study is to evaluate the long-term safety and tolerability of Xanomeline and Trospium Chloride for the treatment of psychiatric disorders in children and adolescents
- Stage
- Phase 3
- Ages
- 5 to 17
- Site
- Advanced Research Center Inc., Anaheim, California
- Locations
- 104 in total
- Run by
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
-
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
- 45 in total
- Run by
- MapLight Therapeutics
-
iTBS to Enhance Social Cognition in People With Psychosis
The goal of this clinical trial is to examine if iTBS applied to the DMPFC improves social cognitive performance compared to sham stimulation in people diagnosed with schizophrenia, schizoaffective disorder, schizophreniform disorder, or psychotic disorder not otherwise specified. The main objectiv…
- Stage
- Not phased
- Ages
- 18 to 39
- Site
- Zucker Hillside Hospital, Glen Oaks, New York
- Run by
- Northwell Health
-
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
- 101 in total
- Run by
- Eli Lilly and Company
-
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
- 37 in total
- Run by
- Bristol-Myers Squibb
-
Acceptability and Feasibility of Work-Oriented Social-Cognitive Skills Training for Veterans With Serious Mental Illness
Many individuals with serious mental illness have difficulty accurately interpreting interpersonal cues and effectively engaging in social exchanges. Difficulties related to the interpersonal aspects of work can lead to isolation, poor productivity, and job loss. The goals of this study are to: 1) …
- Stage
- Not phased
- Ages
- 18 and older
- Site
- Minneapolis VA Health Care System, Minneapolis, MN, Minneapolis, Minnesota
- Run by
- VA Office of Research and Development
-
Safety and Tolerability of Open-Labeled Iloperidone in Adolescents
To evaluate the safety and tolerability of iloperidone in adolescent patients with schizophrenia or bipolar I disorder for up to 52 weeks of treatment.
- Stage
- Phase 4
- Ages
- 12 to 17
- Site
- Vanda Investigational Site, Dothan, Alabama
- Locations
- 11 in total
- Run by
- Vanda Pharmaceuticals
-
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
-
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, Orange, California
- Locations
- 20 in total
- Run by
- Bristol-Myers Squibb
-
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
- 65 in total
- Run by
- Intra-Cellular Therapies, Inc.
-
NBI-1117568-SCZ3030: Evaluation of NBI-1117568 in Inpatient Adults With Schizophrenia
The primary objective for this study is to evaluate the efficacy of NBI-1117568 compared with placebo on improving behavioral and psychological symptoms of schizophrenia in adults.
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Neurocrine Clinical Site, Little Rock, Arkansas
- Locations
- 20 in total
- Run by
- Neurocrine Biosciences
-
NBI-1117568-SCZ3032: Long-Term Evaluation of NBI-1117568 in Adults With Schizophrenia
This study will evaluate the long-term safety of NBI-1117568 in adults with schizophrenia.
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Neurocrine Clinical Site, Bryant, Arkansas
- Locations
- 61 in total
- Run by
- Neurocrine Biosciences
-
Efficacy of NBI-1117568 in Preventing Relapse in Adults With Schizophrenia
The main objective of the study is to evaluate NBI-1117568 compared with placebo in delaying relapse of symptoms of schizophrenia in adults who have a stable response after open-label treatment with NBI-1117568.
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Neurocrine Clinical Site, Garden Grove, California
- Locations
- 25 in total
- Run by
- Neurocrine Biosciences
-
State Representation in Early Psychosis 2
This observational study will examine behavioral and electroencephalography measures related to state representation in individuals with early psychosis and healthy control participants. Participants will complete clinical interviews, self-report measures, cognitive assessments, computerized behavi…
- Stage
- Not phased
- Ages
- 15 to 45
- Site
- University of Minnesota Ambulatory Research Center, Minneapolis, Minnesota
- Locations
- 2 in total
- Run by
- University of Minnesota
-
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
-
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
-
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
-
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
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.