Schizophrenia Clinical Trials in Boston, Massachusetts
13 studies are recruiting for schizophrenia in Boston, Massachusetts 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 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
- Boston Children's Hospital, Boston, Massachusetts
- Locations
- 38 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, Boston, Massachusetts
- Locations
- 42 in total
- Run by
- MapLight Therapeutics
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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
- Boston Children's Hospital, Boston, Massachusetts
- Locations
- 91 in total
- Run by
- Karuna Therapeutics, Inc., a Bristol Myers Squibb company
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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
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 2 in total
- Run by
- Mclean Hospital
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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
- Boston Medical Center, Boston, Massachusetts
- Locations
- 20 in total
- Run by
- Bristol-Myers Squibb
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Search for Novel Transcranial Magnetic Stimulation (TMS) Targets for Mental Illness
Participants will receive Transcranial Magnetic Stimulation (TMS) at a random location in the left prefrontal cortex, excluding sites that are potentially unsafe. Extensive behavioral testing will be conducted to determine which behaviors are modulated by stimulating which circuits.
- Stage
- Phase 2
- Ages
- 18 to 65
- Site
- Brigham and Women's Hospital, Boston, Massachusetts
- Locations
- 2 in total
- Run by
- Brigham and Women's Hospital
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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, Boston, Massachusetts
- Locations
- 57 in total
- Run by
- Neurocrine Biosciences
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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, Boston, Massachusetts
- Locations
- 20 in total
- Run by
- Neurocrine Biosciences
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CLOZAPINE Response in Biotype-1
The CLOZAPINE study is designed as a multisite study across 5 sites and is a clinical trial, involving human participants who are prospectively assigned to an intervention. The study will utilize a stringent randomized, double-blinded, parallel group clinical trial design. B2 group will serve as ps…
- Stage
- Phase 4
- Ages
- 18 to 60
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 5 in total
- Run by
- University of Texas Southwestern Medical Center
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Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services
The Biomarkers/Biotypes, Course of Early Psychosis and Specialty Services (BICEPS) study aims to understand the early stages of psychotic disorders like Schizophrenia, Schizoaffective Disorder, and Bipolar I Disorder. It involves gathering mental health information, brain scans (MRI), eye movement …
- Stage
- Not phased
- Ages
- 18 to 40
- Site
- Beth Israel Deaconess Medical Center, Boston, Massachusetts
- Locations
- 6 in total
- Run by
- Beth Israel Deaconess Medical Center
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Enhanced Coordinated Specialty Care for Early Psychosis
The goal of this clinical trial is to compare engagement in treatment in coordinated specialty care (CSC) to five extra care elements (CSC 2.0) in first-episode psychosis. The main question it aims to answer is: • Does the addition of certain elements of care increase the number of visits in treatm…
- Stage
- Not phased
- Ages
- Any age
- Site
- Massachusetts General Hospital FEPP Clinic, Boston, Massachusetts
- Locations
- 5 in total
- Run by
- Mclean Hospital
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Transcranial Direct Current Stimulation (tDCS) Neuromodulation of Executive Function Across Neuropsychiatric Populations
In the current study, the investigators aim to understand the role of transcranial direct current stimulation (tDCS) in improving executive function across neuropsychiatric populations known to have deficits in this cognitive domain.
- Stage
- Not phased
- Ages
- 18 to 65
- Site
- Massachusetts General Hospital, Boston, Massachusetts
- Run by
- Massachusetts General Hospital
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Safety and Efficacy of Brilaroxazine (RP5063) in Schizophrenia
This study is to evaluate the effect and safety of Brilaroxazine in patients with acute schizophrenia compared to the placebo short and long-term. Brilaroxazine will be given at fixed doses of 15 mg or 50 mg once daily over 4 weeks, then in the long-term flexible doses 15-50mg daily over a period o…
- Stage
- Phase 3
- Ages
- 18 to 65
- Site
- Reviva site, Boston, Massachusetts
- Locations
- 18 in total
- Run by
- Reviva Pharmaceuticals
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.