Recruiting
Phase 3

Brilaroxazine

Sponsor:

Reviva Pharmaceuticals

Code:

NCT05184335

Conditions

Schizophrenia

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Accepted

Interventions

Brilaroxazine

Placebo

Study Details

Brief summary:

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.

Conditions

Schizophrenia

Study ID

NCT05184335

Start date

Jan 24, 2022

Status verified date

Dec, 2024

Completion date

Feb, 2025

Anticipated

Primary completion date

Feb, 2025

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18 - 65

Healthy Volunteers: Accepted

Inclusion Criteria:

1. Subject is male or female, aged 18 to 65 years
2. 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
3. Diagnosis schizophrenia

Exclusion Criteria:

1. Has a history of treatment resistance exhibited by any of the following:

1. No or minimal response to at least 2 periods of treatment lasting 28 days or longer, with antipsychotic agents at the maximally tolerated dose.
2. Lifetime history of clozapine use
3. History of electroconvulsive therapy (ECT) for treatment of schizophrenia within the past 5 years.
2. Is treatment-naïve for schizophrenia.
3. Primary current diagnosis other than schizophrenia or a comorbid diagnosis that is primarily responsible for the current symptoms and functional impairment.
4. Has a current diagnosis of a psychotic disorder other than schizophrenia or a behavioral disturbance thought to be due to substance abuse disorder.
5. Meets criteria for moderate-to-severe substance use disorder within past 6 months prior to Screening (excluding those related to caffeine or nicotine).
6. 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.
7. 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.
8. On antipsychotic within the Screening Period (minimum 3 days prior to Baseline and throughout the study).
9. 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).
10. Antipsychotic depot medication within 5 half-lives prior to Baseline.
11. 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.

Study Design

Enrollment

690 participants

Anticipated

Allocation

Randomized

Intervention Model

Parallel Assignment

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

active comparator: RP5063 15 mg once daily

administered OD for 28 days then flexibly 15-50mg over a period of 52 weeks.

active comparator: RP5063 (brilaroxazine) 50 mg once daily

administered OD for 28 days, then flexibly 15-50mg over a period of 52 weeks

placebo comparator: Placebo

administered OD for 28 days.

Interventions

Brilaroxazine

RP5063, a new chemical entity (NCE), is a novel multimodal neuromodulator intended for treating schizophrenia and comorbid conditions. This drug is an investigational drug and has not been approved for treatment or marketing. RP5063 belongs to a class of third generation antipsychotics called Dopamine-Serotonin System Stabilizers. The chemical name of the RP5063 active pharmaceutical ingredient (API) is 6-(4-(4-(2,3-dichlorophenyl)-piperazin-1-yl)-butoxy)-2H-benzo\[b\]\[1,4\]oxazin-3(4H)-one hydrochloride.

Placebo

RP5063 matching Placebo

Primary outcome measure

  • Double Blind Safety and Efficacy of Brilaroxazine (RP5063) [ Time Frame: 28 days ]
  • Open label Safety and Efficacy of Brilaroxazine (RP5063) [ Time Frame: 52 weeks ]

Central Contacts and Locations

Central contacts

Locations

Reviva site

Recruiting

Phoenix, Arizona, United States, 85012

Reviva site

Recruiting

Bentonville, Arkansas, United States, 72712

Reviva site

Recruiting

Little Rock, Arkansas, United States, 72211

Reviva site

Recruiting

Rogers, Arkansas, United States, 72758

Reviva site

Recruiting

Garden Grove, California, United States, 92845

Reviva site

Recruiting

Lemon Grove, California, United States, 92945

Reviva site

Recruiting

Riverside, California, United States, 92506

Reviva site

Recruiting

Hollywood, Florida, United States, 33021

Reviva site

Recruiting

Hollywood, Florida, United States, 33024

Reviva site

Recruiting

Miami Lakes, Florida, United States, 33016

Reviva site

Recruiting

Atlanta, Georgia, United States, 30331

Reviva site

Recruiting

Decatur, Georgia, United States, 30030

Reviva site

Recruiting

Chicago, Illinois, United States, 60641

Reviva site

Recruiting

Gaithersburg, Maryland, United States, 20877

Reviva site

Recruiting

Boston, Massachusetts, United States, 02114

Reviva site

Recruiting

Oklahoma City, Oklahoma, United States, 73112

Reviva site

Recruiting

Austin, Texas, United States, 78754

Reviva site

Recruiting

Richardson, Texas, United States, 75080

More Information

Sponsor

Reviva Pharmaceuticals

Last update posted

Dec 19, 2024

Last verified

Dec, 2024

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-08. This information was provided to ClinicalTrials.gov by Reviva Pharmaceuticals on 2024-12-19.