ACTIVE_NOT_RECRUITING

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

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

Quick Facts

Study Start:2024-04-18
Study Completion:2026-02
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:ACTIVE_NOT_RECRUITING

Study ID

NCT06256367

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. * Have a physician-confirmed diagnosis of BP-I, with or without comorbidities.
  2. * 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.
  3. * Have a Montgomery-Åsberg Depression Rating Scale (MADRS) score \>= 20 at baseline.
  4. * Have a Functioning Assessment Short Test (FAST) score \>= 21 at baseline.
  5. * Naïve to cariprazine in the current major depressive episode.
  1. * Have a medical or psychiatric condition, or planned surgical procedure, which will interfere with study participation, as judged by the investigator.
  2. * Have a known contraindication to cariprazine including any of the following:
  3. * Hypersensitivity to cariprazine or any ingredient in the formulation
  4. * For all sites, concomitant use of strong cytochrome P450 (CYP) 3A4 inhibitors and inducers
  5. * For Canadian sites, as per country label, concomitant use of moderate CYP 3A4 inhibitors and inducers
  6. * Current major depressive episode duration \> 12 months.

Contacts and Locations

Principal Investigator

ABBVIE INC.
STUDY_DIRECTOR
AbbVie

Study Locations (Sites)

University of Alabama at Birmingham - Main /ID# 260000
Birmingham, Alabama, 35233
United States
Bowman Medical Group /ID# 259989
Beverly Hills, California, 90212-1910
United States
UC Davis /ID# 259723
Sacramento, California, 95817-2310
United States
Montano Wellness LLC /ID# 259837
Cromwell, Connecticut, 06416
United States
Georgia Psychiatric Consultants & Advanced Discovery Research /ID# 259975
Atlanta, Georgia, 30318-3102
United States
Omaha Insomnia and Psychiatric Services /ID# 259961
Omaha, Nebraska, 68144-2359
United States
Quest Therapeutics of Avon /ID# 259838
Avon Lake, Ohio, 44012-1004
United States
North Star Medical Research LL /ID# 259730
Middleburg Heights, Ohio, 44130
United States
Rivus Wellness And Research Institute /ID# 259966
Oklahoma City, Oklahoma, 73112
United States
Betts Psychiatric, PC /ID# 259737
Eugene, Oregon, 97401-6008
United States
Ut Southwestern Medical Center /Parkland Health and Hospital System /Id# 260001
Dallas, Texas, 75235-7709
United States

Collaborators and Investigators

Sponsor: AbbVie

  • ABBVIE INC., STUDY_DIRECTOR, AbbVie

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-04-18
Study Completion Date2026-02

Study Record Updates

Study Start Date2024-04-18
Study Completion Date2026-02

Terms related to this study

Keywords Provided by Researchers

  • Bipolar I Disorder
  • Cariprazine
  • CReW BP-I

Additional Relevant MeSH Terms

  • Bipolar I Disorder