Safety and Efficacy of Brilaroxazine (RP5063) in Schizophrenia

Recruiting Phase 3 Interventional Study
Schizophrenia
Pivotal Trial This treatment is in the last trial phase before FDA approval. Prior Safety Data This treatment has already been tested in at least one earlier human trial. Healthy Volunteers Welcome You do not need to have the condition being studied to take part.
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At a Glance
Age
18 – 65
Sex
Any
Trial phase
Phase 3
Study type
Interventional
Purpose
Treatment
Participants needed
690 (estimated)
Sponsor
Reviva Pharmaceuticals · Industry
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About This Trial

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.

Trial Locations
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Eligibility Criteria
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 Criter…
Contacts

Medical Director

+1 4085018881

medicaldirector@revivapharma.com

CONTACT