MTOR Inhibitors in Older Adults
University of Texas Southwestern Medical Center · with University of Maryland, Baltimore, National Institute on Aging (NIA) · NCT06727305
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 65–80 · All sexes
- Healthy volunteers
- Accepted
- Study type
- Interventional · Phase 1, Phase 2
- Target enrollment
- 60
- US sites recruiting
- 1
- Study start
- May 11, 2026
- Record last updated
- June 25, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
Over the past decades, healthcare systems face significant challenges to meet the needs of an aging population due to progressive debility, functional decline and chronic diseases development. While there is a growing appreciation of the potential impact of mTOR inhibitors on slowing aging processes, preventing chronic disease and prolonging healthy lifespan, a major challenge in developing clinical trials to establish the clinical efficacy of mTOR inhibitors is the absence of pharmacokinetics (PK) and pharmacodynamics (PD) data in older adults. The proposed study will provide the foundation for future clinical trials assessing the role of mTOR inhibitors on aging related indications
Being studied: Sirolimus 0.5 Mg Oral Tablet; Sirolimus 1Mg Oral Tablet; Sirolimus 2 MG Oral Tablet; Everolimus 0.5 MG Oral Tablet; Everolimus 1 MG Oral Tablet; Everolimus 2 MG Oral Tablet
Conditions: Aging
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
Inclusion Criteria
- Community-dwelling adults
- Patients should be 65 Years and older
- Patients is able to understand and follow trial procedures
Exclusion Criteria
- Creatinine clearance \<30 mL/min;
- History of chronic liver disease;
- Uncontrolled Hypertension (i.e., systolic blood pressure >160 mm Hg);
- Hemorrhagic central nervous system (CNS) event within 1 year from screening visit;
- Thrombotic event (DVT,PE) within 1 year from screening visit if not on anticoagulation;
- Planned major surgical procedures;
- Cardiovascular diseases ( i.e., admission for heart failure or myocardial infarction within 12 months);
- Taking medication that increase or decrease sirolimus blood concentrations;
- Other investigational therapy received within 1 month prior to screening visit;
- History of dementia; 11 Dependence in any Katz Basic Activities of Daily Living.
Recruiting US locations
UT Southwestern Medical Center
Dallas, TX 75390
Site contact: Rhoda Annoh Gordon, PharmD, MPH · 2146457108 · Rhoda.annohgordon@utsouthwestern.edu
Study contacts (from the official record)
- Irina Timofte, MD, MS · 2163347534 · Irina.Timofte@utsouthwestern.edu
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