Home › Trials › NCT06658093
Clinical trial Recruiting at 1 site Early Phase 1 Interventional Ages 65 to 90

Restoring youthful mTOR activity in older adults

Official title: RESTOR [Rapamycin and Everolimus Study Towards Older Rejuvenation]: An Exploratory PK/PD Study of mTOR Inhibition in Older Human Subjects

Run by The University of Texas Health Science Center at San Antonio · NCT06658093 · Data updated 2026-11-12

This study will test whether taking rapamycin or everolimus can safely bring mTOR activity in healthy adults aged 65–90 closer to levels seen in younger people.

Quick facts

PhaseEarly Phase 1
Study typeInterventional
Ages65 Years to 90 Years
SexAll
Enrollment194 (estimated)
SponsorThe University of Texas Health Science Center at San Antonio
Academic / other
Drugs / interventionsprednisone
Locations1 site (San Antonio, Texas)
StatusRecruiting
StartedMarch 4, 2026
Main results expectedJuly 2028
Study endsJuly 2028
Registry record updatedJune 1, 2026
Trial IDNCT06658093 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Ideal participants are community-dwelling, generally healthy men and women aged 65–90 with stable medical conditions who can attend in-person visits and give informed consent.

Probably not a fit

People who live in long-term care facilities or who have diabetes, recent cancer treatment, chronic inflammatory or autoimmune disease, or moderate-to-severe heart or lung disease are excluded and unlikely to benefit from this protocol.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

The protocol has three parts: first, measurement of target mTOR activity in untreated young adults to define ‘youthful’ benchmarks. Next, a short-term dose-finding phase in healthy older adults (65–90 years) where different doses and schedules of oral rapamycin or everolimus are given for six weeks with four weeks of follow-up. Finally, a placebo-controlled trial compares daily (sustained) versus intermittent dosing for six months of treatment plus six months of follow-up to test the selected regimen(s). Both sexes are enrolled to identify possible sex-specific dosing differences.

Why it matters

Potential benefit: If successful, the approach could safely restore more youthful mTOR signaling in older adults and potentially reduce age-related functional decline and disease risk.

How similar studies have gone: Animal studies and small human trials have shown mTOR inhibitors can influence aging-related pathways, but large randomized trials testing dosing to restore youthful mTOR levels in healthy older adults are limited.

Who can join: the full rules

Show full inclusion / exclusion criteria 
Inclusion Criteria:

Older Cohort Sub-study 2 (AIM 1) and Sub-study 3 (AIM 2):

1. Age ≥65 to 90 years
2. Men and women
3. In good health with all medical problems stable.
4. Community-dwelling
5. Agreement to adhere to Lifestyle Considerations throughout study duration.
6. Ability of participant to understand and the willingness to sign a written informed consent document.

Exclusion Criteria:

Older Cohort Sub-study 2 (AIM 1) and Sub-study 3 (AIM 2):

1. Resident of nursing home or long-term care facility
2. Subjects with diabetes or currently taking glucose lowering medications
3. History of moderate-severe heart disease (New York Heart Classification greater than grade II) or pulmonary disease (dyspnea on exertion upon climbing one flight of stairs or less; abnormal breath sounds on auscultation); Moderate to severe valvular heart disease
4. Active cancer or history of cancer treatment within the last 5 years
5. Chronic inflammatory condition, autoimmune disease, or infectious processes (e.g., active tuberculosis, HIV, rheumatoid arthritis, systemic lupus erythematosus, acute or chronic hepatitis B or C)
6. History of a coagulopathy or any medical condition requiring anticoagulation (except low dose ASA)
7. Renal insufficiency with an estimated glomerular filtration rate of \<30ml/min
8. Uncontrolled hypercholesterolemia \>350mg/dl or uncontrolled hypertriglyceridemia \>500mg/dl
9. Anemia or abnormal blood cell counts: hemoglobin level \<9.0g.dl; white blood count \<3500/mm3; neutrophil count \<2000/ mm3; platelet count \<125,000/mm3
10. History of skin ulcers or poor wound healing
11. Active tobacco use (within 6 months)
12. Diagnosis of any disabling neurologic disease such as Parkinson's Disease, Amyotrophic Lateral Sclerosis, multiple sclerosis, cerebrovascular accident with residual deficits (muscle weakness or gait disorder), severe neuropathy, diagnosis of dementia or Clox1 score less than 10 at the time of screening visit, cognitive impairment due to any reason such that the patient is unable to provide informed consent
13. Liver disease
14. Systemic treatment with an immunosuppressant (prednisone, etc.) within the year prior to enrollment
15. Treatment with drugs known to affect cytochrome P450 (CYP3A4), i.e., diltiazem, erythromycin.
16. Patients with history of recent (within 6 months) myocardial infarction or active coronary disease
17. Patients with history of recent (within 6 months) intestinal disorders
18. History of severe head trauma, brain injury, brain surgery, inflammation of the brain, or history of seizure disorder
19. History of Long-Covid (PASC) within one year
20. Acute Covid19 or Covid19 infection within the last 6 months
21. Unwilling to forgo grapefruit juice consumption.
22. Participation in mTORi study within the prior year. (Note: participants in AIM 1 will be excluded from participating in AIM 2 of the proposed trial.)
23. Allergic to RAPA or EVERO
24. Allergic to lidocaine
25. Recreational drug use
26. Donated blood over a two-month period prior to study initiation.
27. Currently using cannabidiol (CBD) or tetrahydrocannabinol (THC) or any preparation contained these, or related, substances.
28. Currently using hormone replacement or modulating therapies.

Where it's running

  • The University of Texas Health Science Center at San Antonio
    San Antonio, Texas, United States     Recruiting

Study contacts

  • Principal investigator: Ellen Kraig, PhD — The University of Texas Health Science Center at San Antonio
  • Study coordinator: Dean L Kellogg, Jr, MD PhD
  • Email: kelloggd@uthscsa.edu
  • Phone: (210) 617 5197

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
View on ClinicalTrials.gov ↗ Find more trials like this →
Browse more
Aging 2413The University of Texas Health Science Center at San Antonio 74
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.