Safety and Efficacy of Brilaroxazine (RP5063) in Schizophrenia
Reviva Pharmaceuticals · NCT05184335
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18–65 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 3
- Target enrollment
- 690
- US sites recruiting
- 18
- Study start
- January 24, 2022
- Record last updated
- December 19, 2024
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
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 of 52 weeks.
Being studied: Brilaroxazine; Placebo
Conditions: Schizophrenia
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Subject is male or female, aged 18 to 65 years
- Subject reads, understands, and signs an Institutional Review Board (IRB)/Independent Ethics Committee (IEC)-approved current ICF prior to performing any of the Screening procedures
- Diagnosis schizophrenia
Exclusion Criteria
- Has a history of treatment resistance exhibited by any of the following:
- No or minimal response to at least 2 periods of treatment lasting 28 days or longer, with antipsychotic agents at the maximally tolerated dose.
- Lifetime history of clozapine use
- History of electroconvulsive therapy (ECT) for treatment of schizophrenia within the past 5 years.
- Is treatment-naïve for schizophrenia.
- Primary current diagnosis other than schizophrenia or a comorbid diagnosis that is primarily responsible for the current symptoms and functional impairment.
- Has a current diagnosis of a psychotic disorder other than schizophrenia or a behavioral disturbance thought to be due to substance abuse disorder.
- Meets criteria for moderate-to-severe substance use disorder within past 6 months prior to Screening (excluding those related to caffeine or nicotine).
- Has a history of the following: (a) 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 (CNS) (b) intellectual disability of a severity that would impact ability to participate in the study.
- Subject has a current primary DSM-5 diagnosis other than schizophrenia, including schizoaffective disorder, major depressive disorder, post-traumatic stress disorder, obsessive-compulsive disorder, manic episode, hypomania, panic disorder, delirium, amnestic or other cognitive disorders. Also, subjects with borderline, paranoid, histrionic, schizotypal, schizoid, or antisocial personality disorder.
- On antipsychotic within the Screening Period (minimum 3 days prior to Baseline and throughout the study).
- Within 28 days prior to Baseline: monoamine oxidase (MAO) inhibitors, CNS stimulants, potent CYP3A4/5 enzyme-inducing drugs including but not limited to rifampin and carbamazepine and strong CYP3A4/5 inhibitors like ketoconazole, itraconazole, clarithromycin, etc. (see Appendix 20.1 for prohibited medications).
- Antipsychotic depot medication within 5 half-lives prior to Baseline.
- Positive Urine Drug Screen for drugs of abuse, including amphetamines, barbiturates, cocaine, ecstasy, phencyclidine or opiates meeting criteria of moderate-to-severe DSM-5 substance use disorder.
Recruiting US locations
Reviva site
Phoenix, AZ 85012
Site contact: Coordinator
Reviva site
Bentonville, AR 72712
Site contact: Coordinator
Reviva site
Little Rock, AR 72211
Site contact: Coordinator
Reviva site
Rogers, AR 72758
Site contact: Coordinator
Reviva site
Garden Grove, CA 92845
Site contact: Coordinator
Reviva site
Lemon Grove, CA 92945
Site contact: Coordinator
Reviva site
Riverside, CA 92506
Site contact: Coordinator
Reviva site
Hollywood, FL 33021
Site contact: Coordinator
Reviva site
Hollywood, FL 33024
Site contact: Coordinator
Reviva site
Miami Lakes, FL 33016
Site contact: Coordinator
Reviva site
Atlanta, GA 30331
Site contact: Coordinator
Reviva site
Decatur, GA 30030
Site contact: Coordinator
Reviva site
Chicago, IL 60641
Site contact: Coordinator
Reviva site
Gaithersburg, MD 20877
Site contact: Coordinator
Reviva site
Boston, MA 02114
Site contact: Coordinator
Reviva site
Oklahoma City, OK 73112
Site contact: Coordinator
Reviva site
Austin, TX 78754
Site contact: Coordinator
Reviva site
Richardson, TX 75080
Site contact: Coordinator
Study contacts (from the official record)
- Medical Director · +1 4085018881 · medicaldirector@revivapharma.com
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