Levetiracetam for Persons at Risk for Alzheimer's Disease

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age55-85
SponsorSunnybrook Health Sciences Centre

About this trial

The goal of this clinical trial is to investigate whether very small doses of a drug called levetiracetam (LEV) may reduce abnormal brain signaling in individuals who are at an increased risk for developing Alzheimer's Disease (AD). The study is looking for individuals who have a parent or sibling with Alzheimer's disease (dementia), and who have memory complaints but are currently performing within normal limits on cognitive testing. During the screening period, a functional MRI (fMRI) scan of the brain will identify those participants who have the abnormal brain signaling that the study is looking to treat.

All participants will receive 4 weeks of treatment with LEV and 4 weeks of treatment with placebo (a sugar pill), but it will not be known what order they will receive them in. Participants will undergo cognitive testing, genetic testing, and several brain imaging scans as part of the study.

This is a pilot study, meaning that it is being carried out for the first time in a small number of participants. If the results show that treatment with LEV appears to be more beneficial than placebo in normalizing brain signaling, a larger study may follow.

This study is only being carried out in Toronto, Canada.

Eligibility criteria

Qualifiers

Willing to undergo all study procedures and has signed the informed consent form.

Has a friend or family member who has weekly contact with the participant and is willing to sign the study partner informed consent and complete study questionnaires.

Female participants must be post-menopausal (amenorrheic for at least 12 consecutive months without other known or suspected cause) or surgically sterile (bilateral tubal ligation, total hysterectomy, or bilateral oophorectomy).

Sufficiently fluent in English to undergo cognitive testing, per investigator judgment.

Disqualifiers

History of hypersensitivity to levetiracetam or any other ingredients in the study drug or placebo.

Any type of cognitive impairment

History of transient ischemic attacks within 12 months of Screening

History of seizures within 12 months of Screening

Trial design

Treatments tested in this trial

  • Levetiracetam (LEV)
  • Placebo

Treatment groups

40 Participants
are divided into 2 treatment groups

Sponsors and collaborators

Sunnybrook Health Sciences Centre

Lead sponsor

University Health Network, Toronto

Collaborator

Weston Brain Institute

Collaborator