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NCT04629495Active, not recruitingPhase 2

Rapamycin - Effects on Alzheimer's and Cognitive Health

Rapamycin - Effects on Alzheimer's and Cognitive Health (REACH)

Source: ClinicalTrials.gov · Last updated 9 Jun 2026

Brief summary (registry, in English)

This study will evaluate the safety, tolerability, and feasibility of 12 month oral rapamycin treatment in older adults with amnestic mild cognitive impairment (aMCI) and early stage Alzheimer's disease (AD).

Status (registry)
Active, not recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
40 (actual)
First submitted
9 Nov 2020
Start date
11 Aug 2021
Primary completion date
5 Mar 2026
Lead sponsor
The University of Texas Health Science Center at San Antonio
NCT number
NCT04629495

What you commit to

  • Study type: Interventional · Phase 2
  • Participants enrolled: 40
  • From 11 Aug 2021 to the primary completion date, 5 Mar 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current tobacco or illicit drug use or alcohol abuse
  • Current medications that affect cytochrome 450 3A4 (CYP3A4)
  • Immunosuppressant therapy within the last year
  • Chemotherapy or radiation treatment within the last year
  • Organ transplant recipients

Other illness

  • History of skin ulcers or poor wound healing
  • Current or chronic history of liver or kidney disease or known hepatic or biliary abnormalities
  • Current or chronic history of pulmonary disease or abnormal pulse oximetry (\<90%)
  • Chronic heart failure
  • Recent history (past six months) of myocardial infarction, active coronary artery disease, intestinal disorders, stroke, or transient ischemic attack
  • Significant neurological conditions other than AD or MCI
  • 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 lesion, including mass effect or abnormal intracranial pressure, which would indicate contraindications to lumbar puncture

Lab values

  • Diabetes (HBA1c≥6.5% or antidiabetic medications)
  • Use of anti-platelet or anti-coagulant medications other than aspirin
  • Untreated hypertriglyceridemia (fasting triglycerides \< 250 mg/dl)

Other

  • Pregnancy or lactation
  • Poorly controlled blood pressure (systolic BP\>160, diastolic BP\>90 mmHg - based on two readings)

Who the study is looking for

  • Both genders and all ethnic groups
  • Ages 55 to 89 years
  • Diagnosis of MCI or AD (Mini Mental Status Examination (MMSE): 18-30; Clinical Dementia Rating Scale (CDR) = 0.5 - 1; California Verbal Learning Test III (CVLT-III) Delayed Recall ≤16% based on age-adjusted norms, clinician approval)
  • Amyloid positivity based on Amyloid PET Imaging
  • Labs: Normal blood cell counts without clinically significant excursions; normal liver and renal function; and glucose control (HbA1c \< 6.5%). Fasting lipid panel and prothrombin time/prothrombin time test/international normalized ration (PT/PTT/INR) within normal limits
  • A legally authorized representative (LAR) designated to sign informed consent (if necessary) must attend the Screening visit and accompany the participant to all remaining visits to provide reported outcomes
  • Stable dose of AD medications (Donepezil, rivastigmine, Memantine, galantamine) for at least three months is allowed

Age in the registry: 55 years to 89 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Glenn Biggs Institute for Alzheimer's & Neurodegenerative Diseases
Coordinator of this site? Confirm its status
San AntonioUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.