Observational Study of Oral Cariprazine Capsules to Assess Change in Disease Activity in Adult Participants With Bipolar I Disorder

Last updated: April 17, 2025
Sponsor: AbbVie
Overall Status: Active - Recruiting

Phase

N/A

Condition

N/A

Treatment

N/A

Clinical Study ID

NCT06256367
P24-477
  • Ages > 18
  • All Genders

Study Summary

Bipolar I disorder (BP-I) is a common, chronic, and disabling mental illness with significant morbidity and mortality defined by episodes of mania and depression (or symptoms of both at once, known as mixed features). This prospective, observational study will examine effectiveness, functioning and quality of life outcomes in adult patients with BP-I experiencing a major depressive episode (with or without mixed features) requiring treatment and initiating treatment with cariprazine. It will examine outcomes of cariprazine treatment in a real-world setting in patients with BP-I commonly seen in clinical practices.

Cariprazine (Vraylar) is a medication indicated in the United States and Canada to treat adult patients experiencing manic, mixed or depressive episodes associated with BP-I. This study plans to enroll approximately 170 adult patients with BP-I from the United States and Canada. Cariprazine should be prescribed by the physician under the usual and customary practice of physician prescription. The decision to initiate treatment with cariprazine should be made prior to, and independently from, the patient's decision to participate in the study.

Participants will receive cariprazine as prescribed by their physician. Observational data will be collected during visits which should align to routine standard of care for a duration of up to 24 weeks.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Have a physician-confirmed diagnosis of BP-I, with or without comorbidities.

  • Prescribed cariprazine as part of routine clinical practice with the intention oftreating as per the approved market label, respective country indications, and bythe physician under usual and customary practice of physician prescription.

  • Have a Montgomery-Åsberg Depression Rating Scale (MADRS) score >= 20 at baseline.

  • Have a Functioning Assessment Short Test (FAST) score >= 21 at baseline.

  • Naïve to cariprazine in the current major depressive episode.

Exclusion

Exclusion Criteria:

  • Have a medical or psychiatric condition, or planned surgical procedure, which willinterfere with study participation, as judged by the investigator.

  • Have a known contraindication to cariprazine including any of the following:

  • Hypersensitivity to cariprazine or any ingredient in the formulation

  • For all sites, concomitant use of strong cytochrome P450 (CYP) 3A4 inhibitorsand inducers

  • For Canadian sites, as per country label, concomitant use of moderate CYP 3A4inhibitors and inducers

  • Current major depressive episode duration > 12 months.

Study Design

Total Participants: 170
Study Start date:
April 18, 2024
Estimated Completion Date:
July 31, 2025

Connect with a study center

  • Chatham-Kent Clinical Trials /ID# 262414

    Chatham, Ontario N7L 1C1
    Canada

    Active - Recruiting

  • Grand River Hospital /ID# 263962

    Kitchener, Ontario N2G 1G3
    Canada

    Active - Recruiting

  • Sunny Johnson Medical Research Associates /ID# 267713

    Mississauga, Ontario L5M 4N4
    Canada

    Active - Recruiting

  • Southlake Regional Health Centre /ID# 264212

    Newmarket, Ontario L3Y 2P9
    Canada

    Active - Recruiting

  • START Clinic for Mood and Anxiety Disorders /ID# 262416

    Toronto, Ontario M4W 2N4
    Canada

    Active - Recruiting

  • Institut universitaire en santé mentale de Montréal /ID# 264665

    Montreal, Quebec H1N 3M5
    Canada

    Active - Recruiting

  • Clinique Woodward /ID# 264050

    Sherbrooke, Quebec J1G 2N5
    Canada

    Active - Recruiting

  • Douglas Mental Health University Institute /ID# 262048

    Verdun, Quebec H4H 1R2
    Canada

    Active - Recruiting

  • University of Alabama at Birmingham - Main /ID# 260000

    Birmingham, Alabama 35233
    United States

    Active - Recruiting

  • Bowman Medical Group /ID# 259989

    Beverly Hills, California 90212-1910
    United States

    Active - Recruiting

  • UC Davis /ID# 259723

    Sacramento, California 95817-2310
    United States

    Active - Recruiting

  • CT Clinical Research /ID# 259837

    Cromwell, Connecticut 06416
    United States

    Active - Recruiting

  • Montano Wellness LLC /ID# 259837

    Cromwell, Connecticut 06416
    United States

    Active - Recruiting

  • Georgia Psychiatric Consultants & Advanced Discovery Research /ID# 259975

    Atlanta, Georgia 30318-3102
    United States

    Active - Recruiting

  • Omaha Insomnia and Psychiatric Services /ID# 259961

    Omaha, Nebraska 68144-2359
    United States

    Active - Recruiting

  • Haidar Almhana Nieding LLC /ID# 259838

    Avon Lake, Ohio 44012-1004
    United States

    Active - Recruiting

  • Quest Therapeutics of Avon /ID# 259838

    Avon Lake, Ohio 44012-1004
    United States

    Active - Recruiting

  • North Star Medical Research LL /ID# 259730

    Middleburg Heights, Ohio 44130
    United States

    Active - Recruiting

  • RIVUS Wellness & Research Institute /ID# 259966

    Oklahoma City, Oklahoma 73112-8729
    United States

    Active - Recruiting

  • Rivus Wellness And Research Institute /ID# 259966

    Oklahoma City, Oklahoma 73112
    United States

    Active - Recruiting

  • Betts Psychiatric, PC /ID# 259737

    Eugene, Oregon 97401-6008
    United States

    Active - Recruiting

  • Ut Southwestern Medical Center /Parkland Health and Hospital System /Id# 260001

    Dallas, Texas 75235-7709
    United States

    Active - Recruiting

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