A Randomized, Double-Blind, Placebo-Controlled Study With an Open-Label, Long-Term Safety Phase to Evaluate the Efficacy and Safety of TV-44749 in Adults With Schizophrenia (SOLARIS)
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About
The primary objective of this study is to evaluate the efficacy of TV-44749 in adult participants with schizophrenia.
A key secondary objective is to further evaluate the efficacy of TV-44749 based on additional parameters in adult participants with schizophrenia.
A secondary objective is to evaluate the safety and tolerability of TV-44749 in adult participants with schizophrenia
Another secondary objective of this study is to evaluate the efficacy of TV-44749 from baseline to endpoint in Period 1 in adult participants with schizophrenia.
Total study duration is up to 61 weeks, and treatment duration is up to 56 weeks, with weekly visits during the first 8 weeks and then monthly in-clinic visits with weekly calls during the remainder of the treatment period.
Full description
Participants with exacerbation of schizophrenia may be included. The study will be composed of 2 periods: Period 1 (the double-blind, placebo-controlled, efficacy and safety period) and Period 2 (open-label long term safety period). For each participant, the duration of Period 1 will be 8 weeks, and the duration of Period 2 will be up to 48 weeks. In Period 1, participants will be randomized to one of 3 TV-44749 treatment groups or a placebo group in a 1:1:1:1 ratio. All participants will be randomized again to one of the TV44749 treatment groups in a 1:1:1 ratio for Period 2. The end-of-treatment and follow-up visits will be at 4 and 8 weeks after the last dose of investigational medicinal product administration, respectively.
Enrollment
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Volunteers
Inclusion criteria
- The participant has a current confirmed diagnosis of schizophrenia according to the DSM-5, for >1 year
- The participant has exacerbation of schizophrenia that started ≤8 weeks prior to screening and would benefit from psychiatric hospitalization or continued hospitalization for symptoms of schizophrenia.
- Participants who have received an antipsychotic treatment (other than clozapine) in the past year must have been responsive based on the investigator's judgment (and based on discussions with family members, caregivers, or healthcare professionals, as applicable).
- Body mass index between 18.0 and 40.0 kg/m2, inclusive, at the time of screening
- Women may be included only if they have a negative beta-human chorionic gonadotropin (β-HCG) test at screening and baseline
- Women of childbearing potential must agree not to try to become pregnant, and, unless they have exclusively same-sex partners, must agree to use a highly effective method of contraception prior to the first administration of IMP, and agree to continue the use of this method for the duration of the study, and for 70 days after the last dose of IMP
- The participant is in adequate health as determined by medical and psychiatric history, medical examination, electrocardiogram (ECG), serum chemistry, hematology, coagulation urinalysis, and serology.
- NOTE- Additional criteria apply, please contact the investigator for more information
Exclusion criteria
- The participant has a current clinically significant DSM-5 diagnosis other than schizophrenia (has a primary current diagnosis other than schizophrenia or a comorbid diagnosis that is primarily responsible for the current symptoms and functional impairment).
- The participant has a known history of the following: (a) borderline personality disorder, antisocial personality disorder, or bipolar disorder; (b) traumatic brain injury causing ongoing cognitive difficulties, Alzheimer's disease, or another form of dementia, or any chronic organic disease of the central nervous system; and (c) intellectual disability of a severity that would impact ability to participate in the study.
- The participant was hospitalized for >14 days (with the exception of social or administrative hospitalization) in the current exacerbation episode prior to screening.
- The participant has a significant risk of violent behavior based on the participant's medical history or investigator's judgment.
- The participant has a significant risk of committing suicide based on the participant's medical history or C-SSRS, and the investigator's judgment.
- The participant is currently using an LAI antipsychotic or is still under the coverage period of the specific LAI at time of screening.
- The participant has taken clozapine or has received electroconvulsive therapy within the last 12 months prior to screening.
- The participant is currently receiving daily oral olanzapine at a dose >20 mg/day.
- The participant has current or a history of known hypersensitivity to olanzapine or any of the excipients of TV-44749 or the oral formulation of olanzapine.
- The participant has had a significant sedation or delirium after antipsychotic treatment according to medical and psychiatric history and as judged by the investigator or suffered from delirium due to a medical condition.
- The participant has a non-fasting glucose level of ≥200 mg/dL at screening
- The participant meets criteria for moderate to severe substance use disorder (based on DSM-5 criteria) within the past 6 months (excluding those related to caffeine or nicotine)
- NOTE- Additional criteria apply, please contact the investigator for more information
Trial design
Primary purpose
Allocation
Interventional model
Masking
675 participants in 4 patient groups, including a placebo group
Trial contacts and locations
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Teva U.S. Medical Information
Data sourced from clinicaltrials.gov
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