Low-Dose Adjunctive Brexpiprazole in the Treatment of Bipolar I Depression: An Open-Label Study

Status: Recruiting
Location: See all (3) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 3
SUMMARY

Bipolar disorder (BD) is a frequent and lifelong recurrent mood disorder with treatment-resistant depressive episodes. Importantly, depressive symptoms and cognitive decline are major determinants of functionality and quality of life in this clinical population. There is robust evidence that individuals with BD have neurocognitive deficits (especially in memory and executive functioning domains) compared to the healthy population. These deficits are present in all mood states and can greatly affect patients' functional capacity, often more so than mood symptoms themselves. Many pharmacological treatments for BD adversely affect cognition, and those that are beneficial can be difficult to use. There is thus a pressing need to identify a safe, easy-to-use medication that can target both cognitive deficits and depressive symptoms in BD. It is expected that Brexpiprazole adjunctive treatment will be efficacious in treating BD type I and type II depression by improving mood symptoms, as well as cognitive capacity and global functioning, and that such changes will be accompanied by concurrent alterations in associated brain structures.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 75
Healthy Volunteers: t
View:

• Age: 18-75

• Male or female

• Bipolar Disorder type I or type II

• Current treatment-resistant depressive episode (with MADRS \>/= 24 and item 2 (reported sadness) \>/= 3) for a minimum of 2 weeks but \</= 52 weeks at screening visit and baseline visit

• Patients must have failed at least one other treatment for the current depressive episode

• If female and of childbearing potential, is using an adequate method of contraception. Adequate methods of contraception include abstinence; oral contraceptive pill or surgically implanted device; intra-uterine device; condom plus spermicidal foam or jelly; or tubal ligation

• Is treated with a mood stabilizer (lithium and/or valproate and/or lamotrigine and/or quetiapine \</= 100mg/day)

• The following laboratory values are within normal limits at Screening: CBC with differential; ferritin; extended electrolytes (sodium, potassium, chloride, calcium, magnesium, phosphate); thyroid function test(s); kidney function tests; hemoglobin A1c; lipid profile; prolactin

• Normal EKG at Screening

• Patient is able to give his(her) consent

• Age: 18-75

• Male or female

• No current or past history of any psychiatric disorder

• Patients must have failed at least one other treatment for the current depressive episode

• If female and of childbearing potential, is using an adequate method of contraception. Adequate methods of contraception include abstinence; oral contraceptive pill or surgically implanted device; intra-uterine device; condom plus spermicidal foam or jelly; or tubal ligation

• The following laboratory values are within normal limits at Screening: CBC with differential; ferritin; extended electrolytes (sodium, potassium, chloride, calcium, magnesium, phosphate); thyroid function test(s); kidney function tests; hemoglobin A1c; lipid profile; prolactin

• Normal EKG at Screening

• Patient is able to give his(her) consent

Locations
Other Locations
Canada
McMaster University
TERMINATED
Hamilton
Douglas Mental Health University Institute
RECRUITING
Montreal
Jewish General Hospital
WITHDRAWN
Montreal
Contact Information
Primary
Nada Khalil, BA
nada.khalil.comtl@ssss.gouv.qc.ca
514 444 5397
Backup
Paola Lavin Gonzalez, MD, MSc
maria.lavingonzalez@mail.mcgill.ca
438 389 8181
Time Frame
Start Date: 2021-05-10
Estimated Completion Date: 2025-02
Participants
Target number of participants: 58
Treatments
Experimental: Patient
Individuals diagnosed with Bipolar Disorder Type I or Type II and suffering a major depressive episode who will receive an adjunctive and variable dose of Brexpiprazole treatment
Authors
Benicio Frey, Soham Rej
Related Therapeutic Areas
Sponsors
Collaborators: Jewish General Hospital, McMaster University
Leads: Douglas Mental Health University Institute

This content was sourced from clinicaltrials.gov