Real-life Assessment of Brexpiprazole (Rexulti) in Schizophrenia and in Depressive Disorders

Last updated: July 4, 2025
Sponsor: Dr. Albert Kar-Kin Chung
Overall Status: Active - Recruiting

Phase

N/A

Condition

Schizotypal Personality Disorder (Spd)

Tourette's Syndrome

Psychosis

Treatment

Brexpiprazole

Clinical Study ID

NCT05962216
ReSD-HK
  • Ages 18-65
  • All Genders

Study Summary

Not only being the mainstay of treatment for schizophrenia spectrum psychotic disorders, antipsychotics, especially the second-generation antipsychotics (SGAs) have also been recommended as augmenting agents for treating depression. Dopaminergic agents, including both dopamine D2/D3 antagonists and dopamine partial D2 agonists, have been effective for treating psychosis and schizophrenia. Amongst all SGAs, those with partial D2 agonistic property are generally acknowledged to have better side-effect profiles with lower incidence of extrapyramidal side-effects, prolactin increase, weight gain, QTc prolongation, and metabolic syndrome, as well as more efficacious in alleviating depressive symptoms. Up-to-date, three SGAs, namely aripiprazole, brexpiprazole and cariprazine, are known to possess such partial D2 agonism. ReSD-HK study is part of the ReSD Asian Study aiming to carefully evaluate a cohort of patients prescribed with brexpiprazole on its efficacy and tolerability as treatment for schizophrenia and/or depression in a real-life clinical setting.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Age: 18- 65 years old at the time of enrollment

  • Able to read and communicate in English and/or Chinese

  • Able to give informed consent

  • Has been diagnosed according to Diagnostic and Statistical Manual of MentalDisorders, 5th edition (DSM-5), or International Statistical Classification ofDiseases and Related Health Problems 10th revision (ICD-10) to have either PsychoticDisorders (F10-F19.5, F20-23, F25, F32-F33)

  • is receiving brexpiprazole as treatment for less than 4 weeks at the time ofrecruitment

Exclusion

Exclusion Criteria:

  • Age <18 years old

  • Unable to read English or Chinese

  • Unable to give informed consent

  • Had been diagnosed to have Intellectual Disabilities (DSM-5) or Mental Retardation (ICD-10 F70-73)

Study Design

Total Participants: 40
Treatment Group(s): 1
Primary Treatment: Brexpiprazole
Phase:
Study Start date:
July 01, 2023
Estimated Completion Date:
December 31, 2026

Study Description

This is a 6-month, non-interventional, prospective naturalist study that adult patients (18-65 years old) receiving brexpiprazole for treatment of psychosis and/or as adjunctive treatment for major depressive disorder are eligible to participate. Minimal exclusion criteria are employed to fit the usual real-life setting.

Connect with a study center

  • Queen Mary Hospital

    Hong Kong, 000000
    Hong Kong

    Active - Recruiting

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