Optimized Predictive Treatment In Medications for Unipolar Major Depression (OPTIMUM-D)

PHASE4RecruitingINTERVENTIONAL
Enrollment

400

Participants

Timeline

Start Date

January 20, 2023

Primary Completion Date

December 31, 2028

Study Completion Date

April 30, 2029

Conditions
Major Depressive Disorder
Interventions
DRUG

Escitalopram

All patients will receive open-label escitalopram (10-20 mg/d) for the entire study duration (12 weeks).

DRUG

Brexpiprazole

Depending on the initial randomization process, patients will either receive blinded brexpiprazole (0.5-2 mg/d) for the entire study duration (12 weeks) or for the last 4 weeks of the study if they received the placebo during the first 8 weeks of the study and were non-responders.

Trial Locations (7)

T2N 2T9

NOT_YET_RECRUITING

University of Calgary, Calgary

V6T2A1

NOT_YET_RECRUITING

University of British Columbia, Vancouver

B3H 2E2

RECRUITING

Nova Scotia Health Authority, Halifax

L8P3B6

NOT_YET_RECRUITING

McMaster University, Hamilton

K7L4X3

NOT_YET_RECRUITING

Queen's University, Kingston

M5T2S8

NOT_YET_RECRUITING

University Health Network, Toronto

M6J1H4

NOT_YET_RECRUITING

Centre for Addiction and Mental Health, Toronto

All Listed Sponsors
collaborator

Unity Health Toronto

OTHER

collaborator

Centre for Addiction and Mental Health

OTHER

collaborator

McMaster University

OTHER

collaborator

Queen's University

OTHER

collaborator

University of Ottawa

OTHER

collaborator

University of British Columbia

OTHER

collaborator

University of Calgary

OTHER

collaborator

McGill University

OTHER

collaborator

Dalhousie University

OTHER

collaborator

University of Michigan

OTHER

collaborator

Simon Fraser University

OTHER

lead

Nova Scotia Health Authority

OTHER