Neuroactive Steroid to Treat Depressed Mood: A Trial for People With HIV

Prior treatment

• History of allergic reaction or side effects with prior pregnenolone use
• Currently using testosterone enanthate, testosterone cypionate, or estrogen containing preparations that significantly increase systemic estrogen levels, including but not limited to oral and transdermal forms of estrogen. All other forms of exogenous sex steroid hormones will be evaluated at the discretion of the PI and/or clinical delegates.
• Currently using systemic immunosuppressive agents, including corticosteroids, chemotherapy, or specific immunomodulating agents, such as monoclonal antibodies and TNF-inhibitors
• \<70% adherence to study drug prior to randomization
• Concurrent participation in another interventional trial, except for lifestyle and device studies (For vaccination studies, individuals in the observation period are not exclusionary. Other interventions will be evaluated at the discretion of the PI and/or clinical delegates.)

Other illness

• Recent severe infections including opportunistic infections, active bacterial, mycobacterial, fungal, or certain viral infections
• Vulnerable populations (e.g., pregnant/nursing, severe cognitive or intellectual impairment, incarcerated)
• Any severe (life-threatening or unstable) medical condition as determined by clinician assessment
• Severe renal disease (estimated glomerular filtration rate ≤ 30 mL/min/1.73m2)
• Seizure disorder requiring antiepileptic treatment
• Excessive alcohol or other substances use that would interfere with classification of major depression disorder, study procedures and/or follow-up
• Current diagnosis of bipolar disorder
• Diagnosis of a psychotic disorder (current or lifetime)

Lab values

• Decompensated cirrhosis, active liver inflammation (alanine aminotransferase (ALT)/aspartate aminotransferase (AST) ≥ 5 times the upper limit of normal) or unsuppressed viral hepatitis B or C infection

Other

• Contraindication to magnetic resonance imaging (MRI) or poor-quality baseline MRI preventing image analyses as determined by radiologist assessment
• Use of cobicistat or ritonavir
• High risk for suicide (active suicidal ideation (SI) with plan/intent as assessed by using the Columbia Suicide Severity Rating (C-SSRS) or \> 2 attempts in lifetime or any in the past 6 months) or expresses homicidal ideation necessitating clinical intervention or representing an imminent concern
• Blood pressure, with the lowest reading taken after three repeat readings during screening visit, ≥ 160 mmHg systolic OR ≥ 95 mmHg diastolic or other life-threatening vital signs as determined by clinician assessment
• Clinically significant abnormalities in physical examination or ECG that would interfere with study participation
• Diagnosis of schizophrenia (current or lifetime)
• Inability to swallow pills/capsules
• Not able to complete neuropsychological testing in English

• 18-85 years
• HIV-1 viral load \<200 copies/mL on antiretroviral therapy (ART) at screening visit
• Center for Epidemiological Studies - Depression (CES-D) score ≥ 20