University of Missouri
Columbia, Missouri, 65212, United States
Location contact
Ai-Ling Lin, PhD
PRINCIPAL_INVESTIGATOR
Kim Ray
CONTACT
Nathan Bresette
CONTACT
NCT Number: NCT07728175
Alzheimer's disease is a devastating neurodegenerative disease characterized by accumulation of clumps (also called plaques) and bundles of fibers (also called tangles) in the brain, for which there is currently no cure.
Sirolimus (Rapamycin) is an FDA-approved medication which may improve the blood flow to the brain. The purpose of the clinical trial is to find out whether sirolimus can help improve blood flow and energy use in the brain in women ages 45 to 65 who have the ApoE4 gene, a gene which increases the risk of developing Alzheimer's disease later in life.
There will be two arms in this trail, a sirolimus arm and a placebo arm. A placebo is a pill that looks like the study drug, but it does not have any real medicine in it. Participants will be randomized to one arm or the other, but not to both arms. Three study visits over a 12-week period are required.
Participants will: (i) Complete some questionnaires about how well you think; (ii) Complete genetic testing for the ApoE4 gene; (iii) Have blood work, blood pressure and height and weight collected; (iv) Take either Sirolimus or a placebo daily, by mouth, for approximately 4 weeks; (v) Keep a diary of when the sirolimus or placebo is taken; (vi) Complete 2 Magnetic Resonance Imaging (MRI) exams
Trial opening soon.
Get Notified45 year–65 year
Female
Interventional
Phase 1
Columbia, Missouri, 65212, United States
Ai-Ling Lin, PhD
PRINCIPAL_INVESTIGATOR
Kim Ray
CONTACT
Nathan Bresette
CONTACT
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Participants in Sirolimus arm will receive Sirolimus.
Participants in the Placebo arm will receive Placebo
Time frame: Baseline to 4 weeks
Rate of blood perfusion expressed as mL/100g/min globally and regionally
Time frame: Baseline to 4 weeks
Time frame: Baseline to 4 weeks
Time frame: Baseline to 4 weeks
Time frame: Baseline to 4 weeks
Time frame: Baseline to 4 weeks
Time frame: Baseline to 4 weeks
Glucose uptake in the brain globally and regionally
Contact information is provided by the study sponsor or research team.
University of Missouri-Columbia
Other
Effects of Sirolimus on Middle Aged Asymptomatic ApoE4 Carriers
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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