Dynamic Neural Mechanisms of Brexanolone-induced Antidepressant Effects in Postpartum Depression

Completed

Brief Summary: This is a feasibility study of performing repeated EEG recordings and assessment of affective states during open-label administration of BRX to women with postpartum depression. Study phases will include screening, enrollment, intervention, and follow-up. Subjects will be screened for study eligibility criteria through clinical assessments and self-report. Enrolled subjects will be admitted to the UNC Women's Hospital, where five serial EEG recordings will be obtained, along with frequent assessments of affective state, before, during, and after a 60-hour IV infusion of BRX. Follow-up procedures will include assessments of PPD and affective symptoms, as well as an exit interview with the study team. If feasibility outcomes are achieved, exploratory EEG analyses will be performed with AMICA (adaptive mixture independent component analysis), community detection, and microstate assessment. Exploratory analyses of data collected by facial expression detection software (iMotions Affectiva) are also planned.

Recruitment & Eligibility

Inclusion Criteria

Signed informed consent.
Documented proof of full COVID-19 vaccination
Ambulatory, female, aged 18-45
≤ 8 months postpartum
Agrees to adhere to the study requirements.
Onset of depression in 3rd trimester or within 4 weeks of delivery
Meets DSM-V criteria for major depressive disorder with peripartum onset.
17-item HAM-D total score ≥20 at screening
Stopped breastfeeding or agrees to temporarily stop for 7 days including 4 days of hospitalization and 3 days after
No new psychotropic drugs during screening and active treatment of study
Stable use of any current psychotropic drugs for at least 28 days prior to enrollment, with stable dosage for at least 14 days prior to enrollment
Must be on documented contraceptive.
Must have a caregiver or family member with them to help care for the subject's child(ren) during the infusion and to be in the room with the subject if the child(ren) are present during the infusion

Exclusion Criteria

Positive pregnancy test at screening or day 1
Pregnancy that resulted in a stillbirth, termination, or child that was placed for adoption.
Renal impairment or failure, hepatic impairment or failure, or anemia
Untreated or inadequately treated hypothyroidism or hyperthyroidism
Known allergy to progesterone or allopregnanolone.
Suicide attempt at this episode
Medical history of schizophrenia, and/or schizoaffective disorder
Current psychotic symptoms including delusions, hallucinations, or formal thought disorder.
Concurrent substance abuse
Exposure to another investigational medication or device within 30 days
Has previously participated in any study employing brexanolone or SAGE-217.
Subject is investigative site personnel, sponsor personnel, or an immediate member of their family.
Has received electroconvulsive therapy during current episode.
History of seizure disorder
On anticonvulsant agents
On benzodiazepines

Primary Outcome Measures

Name	Time	Method
Number of Successfully Analyzed EEG Recordings	4 days	Feasibility of EEG recordings. Each participant was scheduled to have 5 EEG recordings.
Number of Subjects Completing the Entire Study Protocol Through the Follow-up Phase	30 days	Feasibility of study completion
Number of Subjects Withdrawn From Protocol Due to Adverse Events or Participation Burden	30 days	Feasibility of subject burden