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NCT Number: NCT07728175

Effects of Sirolimus on Asymptomatic ApoE4 Carriers

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

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Key information

Age range

45 year–65 year

Sex eligibility

Female

Study type

Interventional

Phase

Phase 1

Primary location

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Willing and able to provide informed consent
  • Sex assigned at birth: female
  • 45-65 years old
  • Able to perform self-care and activities of daily living with no or minimal assistance
  • Post-menopausal status or use of highly effective contraception. Post-menopausal is defined as either
  • 12 months of spontaneous amenorrhea with an appropriate clinical profile (e.g., age-appropriate, history of vasomotor symptoms)
  • surgical bilateral oophorectomy (with or without hysterectomy), total hysterectomy, or tubal ligation at least 6 weeks prior to screening. For oophorectomy alone, post-menopausal status must be confirmed by follow-up hormone level assessment
  • Highly effective contraception includes intrauterine devices (IUD), oral contraceptives, or other hormonal contraceptives including injectables, transdermal patches, implants or vaginal rings, or refraining from heterosexual intercourse during the 4 weeks of taking the study drug and for 2 weeks after no longer taking the study drug
  • Body weight of ≥ 40 kg
  • Ability to effectively communicate with the investigator and comply with study requirements

Exclusion criteria

  • Diagnosis of mild cognitive impairment (MCI), dementia, or Alzheimer's disease
  • BMI ≥ 35 (based on MRI feasibility)
  • Type 1 diabetes or poorly controlled type 2 diabetes (HbA1c ≥ 6.5%)
  • History of skin ulcers or poor wound healing
  • Current tobacco or illicit drug use or alcohol abuse (defined as ≥ 3 per day or ≥ 7 per week for women) (Per NIAAA guidelines)
  • Use of anti-platelet or anti-coagulant medications other than aspirin
  • Required use of medications that affect cytochrome P450 3A4 (CYP3A4) or alter cerebral blood flow (see Appendix 1 for tables of excluded medications)
  • Immunosuppressant therapy within the last year
  • Chemotherapy or radiation treatment within the last year
  • Current or chronic history of liver or kidney disease or known hepatic or biliary abnormalities
  • Untreated hypertriglyceridemia (fasting triglycerides < 300 mg/dl)
  • Current or chronic significant history of pulmonary disease
  • Chronic heart failure
  • Pregnancy or lactation
  • Recent history (past six months) of myocardial infarction, active coronary artery disease, intestinal disorders, stroke, or transient ischemic attack
  • Poorly controlled blood pressure (systolic BP > 160 or diastolic BP > 100 mmHg)
  • Active inflammatory, COVID-19, autoimmune, infectious, hepatic, gastrointestinal, malignant, and/or severe mental illness
  • History of, or MRI, or CT positive for, any space occupying brain lesion, including mass effect or abnormal intracranial pressure
  • Organ transplant recipients
  • History of Stroke
  • History of ruptured intracranial aneurysm
  • History of malignancy within the past 2 years, with the following exceptions:
  • Localized basal cell or squamous cell carcinoma of the skin
  • Prostate cancer confined to the gland (AJCC stage T2N0M0 or better)
  • Cervical carcinoma in situ
  • Breast cancer localized to the breast
  • History of epilepsy

Treatment and study plan

Sirolimus (rapamycin)

Drug

Participants in Sirolimus arm will receive Sirolimus.

Placebo

Drug

Participants in the Placebo arm will receive Placebo

Primary outcomes

  1. Change in Cerebral Blood Flow as measured by MRI

    Time frame: Baseline to 4 weeks

    Rate of blood perfusion expressed as mL/100g/min globally and regionally

Secondary outcomes

  1. Measure the change in plasma Marker-cytokine using a Meso Scale Discovery (MSD) analyzer.

    Time frame: Baseline to 4 weeks

  2. Measure baseline to post-treatment changes in Plasma Markers-AD pathology using a Meso Scale Discovery (MSD) analyzer

    Time frame: Baseline to 4 weeks

  3. Measure brain function connectivity by fMRI

    Time frame: Baseline to 4 weeks

  4. Measurement of blood brain barrier by MRI

    Time frame: Baseline to 4 weeks

  5. Measurement of brain oxygenation by MRI

    Time frame: Baseline to 4 weeks

  6. Measurement of glucose uptake in the brain by PET imaging

    Time frame: Baseline to 4 weeks

    Glucose uptake in the brain globally and regionally

Study contacts

Contact information is provided by the study sponsor or research team.

Kim Ray

CONTACT

[email protected]

573-884-5372

Nathan Bresette

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

University of Missouri-Columbia

Other

Registry information

Official study title

Effects of Sirolimus on Middle Aged Asymptomatic ApoE4 Carriers

Important dates

Study start
2026
Primary completion
2027
Study completion
2028
First posted
Jul 27, 2026
Registry last updated
Jul 30, 2026

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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