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NCT06256367Completed

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

Cariprazine Real-world Use in Bipolar I Disorder: Effectiveness, Functioning, Quality of Life, and Tolerability

Source: ClinicalTrials.gov · Last updated 24 Feb 2026

Brief summary (registry, in English)

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.

Status (registry)
Completed
Study type
Observational
Enrollment
120 (actual)
First submitted
5 Feb 2024
Start date
18 Apr 2024
Primary completion date
23 Jan 2026
Lead sponsor
AbbVie
NCT number
NCT06256367

What you commit to

  • Study type: Observational
  • Participants enrolled: 120
  • From 18 Apr 2024 to the primary completion date, 23 Jan 2026
  • 19 sites in 2 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • 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 inhibitors and inducers
    • For Canadian sites, as per country label, concomitant use of moderate CYP 3A4 inhibitors and inducers

Other illness

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

Other

  • Current major depressive episode duration \> 12 months.

Who the study is looking for

  • Have a physician-confirmed diagnosis of BP-I, with or without comorbidities.
  • Prescribed cariprazine as part of routine clinical practice with the intention of treating as per the approved market label, respective country indications, and by the 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.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (19)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Chatham-Kent Clinical Trials /ID# 262414
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ChathamCanadaUnknown status
Grand River Hospital /ID# 263962
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KitchenerCanadaUnknown status
Sunny Johnson Medical Research Associates /ID# 267713
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MississaugaCanadaUnknown status
Institut universitaire en santé mentale de Montréal /ID# 264665
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MontrealCanadaUnknown status
Southlake Regional Health Centre /ID# 264212
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NewmarketCanadaUnknown status
Clinique Woodward /ID# 264050
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SherbrookeCanadaUnknown status
START Clinic for Mood and Anxiety Disorders /ID# 262416
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TorontoCanadaUnknown status
Douglas Mental Health University Institute /ID# 262048
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VerdunCanadaUnknown status
Georgia Psychiatric Consultants & Advanced Discovery Research /ID# 259975
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AtlantaUnited StatesUnknown status
Quest Therapeutics of Avon /ID# 259838
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Avon LakeUnited StatesUnknown status
Bowman Medical Group /ID# 259989
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Beverly HillsUnited StatesUnknown status
University of Alabama at Birmingham - Main /ID# 260000
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BirminghamUnited StatesUnknown status
Montano Wellness LLC /ID# 259837
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CromwellUnited StatesUnknown status
Ut Southwestern Medical Center /Parkland Health and Hospital System /Id# 260001
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DallasUnited StatesUnknown status
Betts Psychiatric, PC /ID# 259737
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EugeneUnited StatesUnknown status
North Star Medical Research LL /ID# 259730
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Middleburg HeightsUnited StatesUnknown status
Rivus Wellness And Research Institute /ID# 259966
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Oklahoma CityUnited StatesUnknown status
Omaha Insomnia and Psychiatric Services /ID# 259961
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OmahaUnited StatesUnknown status
UC Davis /ID# 259723
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SacramentoUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.