Allopregnanolone for Mild Cognitive Impairment Due to Alzheimer's Disease or Mild AD

• Each dose group will be comprised of 8 participants (6 randomized to allopregnanolone; 2 randomized to placebo) administered one dose of allopregnanolone or placebo once per week for 12 weeks. A higher dose will be administered to the next group of participants when the lower dose is shown to be safe and tolerable. 2) Pharmacokinetic analyses will be conducted on blood samples taken from participants at the beginning and end of the trial. 3) The trial will assess safety including via MRI brain imaging.

Inclusion criteria

• Men or postmenopausal women
• 55 years of age or older
• Diagnosis of MCI due to AD or mild AD
• MMSE > 20 at screen
• Capacity to provide informed consent
• Residing in the community with a caregiver able to accompany the patient to clinic visits
• No medical contraindications to participation
• Willingness to comply with study procedures

Exclusion criteria

• Use of benzodiazepines, sedative/hypnotics, anticonvulsants, antipsychotics, and other drugs that might interact with the GABA-A receptor complex
• Seizure disorder, history of stroke, focal brain lesion, traumatic brain injury, substance abuse, malignancy
• Clinically significant laboratory or ECG abnormality
• MRI indicative of any other significant abnormality, including but not limited to evidence of a cerebral contusion, encephalomalacia, aneurysms, vascular malformations, subdural hematoma, or space occupying lesions
• Any condition that would contraindicate an MRI such as the presence of metallic objects in the eyes, skin, heart, or body