Schizophrenia Clinical Trials in Atlanta, Georgia

21 studies are recruiting for schizophrenia in Atlanta, Georgia 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

  1. 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
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    59 in total
    Run by
    Karuna Therapeutics, Inc., a Bristol Myers Squibb company
  2. 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
    CenExel, Atlanta, Georgia
    Locations
    23 in total
    Run by
    LB Pharmaceuticals Inc.
  3. 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
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    38 in total
    Run by
    Bristol-Myers Squibb
  4. 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
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    103 in total
    Run by
    Eli Lilly and Company
  5. 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
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    8 in total
    Run by
    Bristol-Myers Squibb
  6. 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, Atlanta, Georgia
    Locations
    42 in total
    Run by
    MapLight Therapeutics
  7. 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
    CenExeli Research LLC, Atlanta, Georgia
    Locations
    64 in total
    Run by
    Intra-Cellular Therapies, Inc.
  8. 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
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    91 in total
    Run by
    Karuna Therapeutics, Inc., a Bristol Myers Squibb company
  9. 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
    Synexus Clinical Research US Inc, Atlanta, Georgia
    Locations
    8 in total
    Run by
    Janssen Research & Development, LLC
  10. 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
    Emory University., Atlanta, Georgia
    Locations
    55 in total
    Run by
    Bristol-Myers Squibb
  11. 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, Atlanta, Georgia
    Locations
    5 in total
    Run by
    BioXcel Therapeutics Inc
  12. A Trial of the Efficacy and Safety of SEP-363856 in Acutely Psychotic Participants With Schizophrenia

    Evaluate the efficacy and safety of Ulotaront (SEP-363856) in acutely psychotic subjects with schizophrenia

    Stage
    Phase 3
    Ages
    18 to 65
    Site
    Synexus Clinical Research US Inc - Atlanta, Atlanta, Georgia
    Locations
    73 in total
    Run by
    Otsuka Pharmaceutical Development & Commercialization, Inc.
  13. 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, Atlanta, Georgia
    Locations
    57 in total
    Run by
    Neurocrine Biosciences
  14. 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, Atlanta, Georgia
    Locations
    20 in total
    Run by
    Neurocrine Biosciences
  15. Anti-Inflammatory Challenge in Schizophrenia

    This study aims to illuminate the biological underpinnings of negative symptoms in schizophrenia-particularly motivational impairments-by probing the link between systemic inflammation and neural activity in reward-related brain circuits. The primary goal of this study is to determine: * Ventral St…

    Stage
    Phase 4
    Ages
    18 to 55
    Site
    Grady Memorial Hospital, Atlanta, Georgia
    Locations
    2 in total
    Run by
    Emory University
  16. 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, Atlanta, Georgia
    Locations
    15 in total
    Run by
    Neurocrine Biosciences
  17. NBI-1117568-SCZ3029: 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, Atlanta, Georgia
    Locations
    21 in total
    Run by
    Neurocrine Biosciences
  18. Randomized Withdrawal Study in Patients With Schizophrenia

    The purpose of this research is to evaluate the efficacy of dosing iloperidone long-acting injection (LAI) compared to placebo in preventing the exacerbation of symptoms in patients with schizophrenia.

    Stage
    Phase 3
    Ages
    18 to 65
    Site
    Vanda Investigational Site, Atlanta, Georgia
    Locations
    22 in total
    Run by
    Vanda Pharmaceuticals
  19. Efficacy and Safety of Cariprazine in the Treatment of Adolescent Participants (13 to 17 Years of Age) With Schizophrenia

    The purpose of this study is to evaluate the efficacy and safety of cariprazine in the treatment of schizophrenia in the adolescent population.

    Stage
    Phase 3
    Ages
    13 to 17
    Site
    Atlanta Center for Medical Research, Atlanta, Georgia
    Locations
    57 in total
    Run by
    Gedeon Richter Plc.
  20. 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, Atlanta, Georgia
    Locations
    9 in total
    Run by
    Vanda Pharmaceuticals
  21. 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, Atlanta, Georgia
    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.