Actively Recruiting

Phase 2
Age: 65Years - 80Years
All Genders
Healthy Volunteers
NCT05237687

The Role of Sirolimus in Preventing Functional Decline in Older Adults

Led by Irina Timofte · Updated on 2026-02-03

10

Participants Needed

1

Research Sites

91 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Aging is associated with progressive impairment of tissue and organ function, resulting in increased susceptibility to chronic disease, frailty and disability. Currently there are limited treatment options to alter this inevitable process. The proposed work has the potential to identify a new therapeutic intervention to decrease aging-related degenerative processes. Rapamycin or sirolimus is a macrocyclic immunosuppressive drug that inhibits the mammalian target of rapamycin (mTOR). The mammalian target of rapamycin (mTOR) pathway is part of phosphoinositide 3-kinase (PI3K)/protein kinase B (AKT)/mammalian target of rapamycin (mTOR)-dependent pathway which is a fundamentally linked to cell metabolism, proliferation, differentiation, and survival. This pathway is altered in a variety of diseases, including cancers, immunosuppressed states, and fibroproliferative diseases. The mTOR kinase is considered one of the leading regulators of this pathway. Changes in mTOR signaling are closely associated with inflammation, cell growth and survival, leading to the development of chronic diseases. Recent evidence also suggests that mTOR inhibitors are promising modulators of the aging process by slowing the mechanisms of aging at the cellular level. There is a growing appreciation of the potential impact of sirolimus in slowing aging processes and in prolonging healthy lifespan. The proposed study addresses critical gaps in our understanding of the safety and efficacy of sirolimus in delaying aging processes and is based on findings in animal studies and incidental clinical observations. The investigators will overcome potential biases with a randomized control trial. The proposed intervention study is intended to improve our insight into clinical outcomes leading to prevention of chronic diseases such as skin cancer and mortality. Our overarching hypothesis is that sirolimus is one of the first pharmacological agents that will impact the aging process and chronic disease development. Specifically, the investigators aim to investigate whether sirolimus can reduce the occurrence or increase in biomarkers of aging processes.

CONDITIONS

Official Title

The Role of Sirolimus in Preventing Functional Decline in Older Adults

Who Can Participate

Age: 65Years - 80Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 65 to 80 years
  • Women who are postmenopausal or have had surgical sterilization
  • Able to provide informed consent
Not Eligible

You will not qualify if you...

  • Creatinine clearance less than 30 mL/min
  • Chronic liver disease
  • Received other investigational therapy within 1 month before screening
  • Pulmonary Arterial Hypertension with mean Pulmonary Arterial Pressure over 30 mm Hg
  • Extrapulmonary physiological restrictions such as chest wall abnormalities or large pleural effusion
  • Cardiovascular diseases including recent myocardial infarction (within 6 months), planned coronary intervention, or left ventricular ejection fraction below 45%
  • History of hemorrhagic central nervous system event within 1 year
  • Recent serious bleeding or injury events within 3 months such as hemoptysis, hematuria, active gastrointestinal bleeding or ulcers, major injury, or surgery
  • History of thrombotic events including deep vein thrombosis, pulmonary embolism, stroke, or transient ischemic attack within 1 year
  • Other diseases interfering with testing or putting patient at risk during trial
  • Planned major surgical procedures
  • Women who are pregnant, nursing, or planning pregnancy during the trial
  • Active alcohol or drug abuse
  • Significant cognitive impairment
  • Functional impairment affecting activities of daily living
  • Unable to understand or follow trial procedures

AI-Screening

AI-Powered Screening

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Trial Site Locations

Total: 1 location

1

UT Southwestern Medical Center

Dallas, Texas, United States, 75390

Actively Recruiting

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Research Team

I

Irina Timofte

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

PREVENTION

Number of Arms

2

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