Status:
RECRUITING
An Open Label Pilot Study of IV Brexanolone for the Treatment of Post-Traumatic Stress Disorder
Lead Sponsor:
Donald Jeffrey Newport
Collaborating Sponsors:
Sage Therapeutics
Conditions:
Post-Traumatic Stress Disorder
Eligibility:
FEMALE
18-50 years
Phase:
PHASE4
Brief Summary
Open-label study of brexanolone infusion for the treatment of posttraumatic stress disorder in 20 adult women with PTSD. Primary Objective: To determine if brexanolone injection infused intravenousl...
Detailed Description
Study Design and Methodology: Open label study enrolling 20 subjects in which diagnosis of PTSD will be established, PTSD and depressive symptom severity will be assessed with validated psychometric ...
Eligibility Criteria
Inclusion
- Subject has signed an ICF prior to any study-specific procedures being performed
- Subject is a premenopausal female between 18 and 50 years of age, inclusive
- Subject has a current diagnosis of PTSD associated with civilian (i.e., non-military) trauma according to Diagnostic and Statistical Manual of Mental Disorders, 5th edition (DSM-5) and confirmed by the Mini International Neuropsychiatric Interview (MINI) at the screening visit.
- PCL-5 total score ≥ 33 at screening and baseline (Day 0)
- Subject is in good physical health and has no clinically significant findings, as determined by the Investigator, on physical examination, 12-lead ECG, or clinical laboratory tests
- Subject agrees to adhere to the study requirements
- Subject must have a negative pregnancy test at screening and Day 1 prior to the start of study drug infusion
- Subject is willing at screening to delay the start of any new pharmacotherapy regimens, including antidepressant or anti-anxiety medication, until the study drug infusion and 72-hour assessments have been completed; if the subject is taking psychotropic medications, these must be at a stable dose from 14 days prior to screening until the 72-hour assessments have been completed.
- Fluency (oral and written) in the language in which standardized tests will be administered.
- Subject must use one of the following methods of birth control during participation in the study and for 30 days following the end of the study drug infusion:
- Total abstinence (no sexual intercourse)
- Hormonal contraceptives (birth control) including birth control pills, implantable or injectable contraceptives (Norplant® or DepoProvera®)
- A barrier form of contraception such as a condom or occlusive cap with a spermicide
- An intrauterine device
Exclusion
- Subject is currently pregnant, breastfeeding, or postpartum less than 6 months since end of pregnancy
- Subject has renal failure requiring dialysis or fulminant hepatic failure or is anemic (hemoglobin ≤10 g/dL)
- Known allergy to progesterone or allopregnanolone or any other neuroactive steroid GABAA receptor modulator.
- Active psychosis per Investigator assessment
- At risk for suicide in the opinion of the investigator or answers "yes" to "Suicidal Ideation" Item 4 or 5 on the CSSRS (at the time of evaluation) at the screening visit
- Medical history of bipolar disorder, schizophrenia, and/or schizoaffective disorder.
- History of an active substance use disorder in the 6 months prior to screening. A positive urine drug screen (except benzodiazepines under certain circumstances is exclusionary.
- History of seizure disorder.
- Subject has previously been treated with brexanolone or participated in any study employing SAGE-547, SAGE-217, SAGE-324, or SAGE-718.
- Concomitant treatment with benzodiazepines or other CNS depressants; initiation of any psychotropic agents within 14 days of screening.
- Any current or recent medical, psychiatric or social condition which in the investigator's opinion is likely to interfere with the conduct of the study, confound the interpretation of study results, or endanger the subject's well-being. This includes (but is not limited to) any clinically significant oncologic, hematologic, endocrine/metabolic, cardiovascular, respiratory, renal, hepatic, gastrointestinal, infectious or
Key Trial Info
Start Date :
June 1 2023
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
March 1 2026
Estimated Enrollment :
20 Patients enrolled
Trial Details
Trial ID
NCT05254405
Start Date
June 1 2023
End Date
March 1 2026
Last Update
May 22 2024
Active Locations (1)
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1
University of Texas at Austin Dell Medical School
Austin, Texas, United States, 78712